16-2256668-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256668
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256668
    reference: chr 16
allele count: 1
allele frequency: 8.456802652053312e-6
allele num: 118248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.344+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.520G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000566653
  gene symbol: MLST8
  hgvsc: ENST00000566653.1:n.530G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+8G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+8G>T
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.344+8G>T
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

16-2256679-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256679
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256679
    reference: chr 16
allele count: 1
allele frequency: 8.60037497634897e-6
allele num: 116274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.447G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.344+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.344+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.844G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.445G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+19G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.531G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+19G>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP

16-2256684-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256684
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256685
    reference: chr 16
allele count: 1
allele frequency: 8.67995278105687e-6
allele num: 115208
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.455dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000566653
  gene symbol: MLST8
  hgvsc: ENST00000566653.1:n.549dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.539dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.453dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.852dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.344+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.344+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+27dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+27dupC
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

16-2256686-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256686
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256686
    reference: chr 16
allele count: 2
allele frequency: 1.738223535546671e-5
allele num: 115060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.538C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.344+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.851C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.452C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.344+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+26C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+26C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum

16-2256687-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256687
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256687
    reference: chr 16
allele count: 1
allele frequency: 8.717939776472025e-6
allele num: 114706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.344+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.455C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.852C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.453C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.344+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.539C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+27C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

16-2256688-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256688
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256688
    reference: chr 16
allele count: 4
allele frequency: 3.494182186659213e-5
allele num: 114476
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000566653
  gene symbol: MLST8
  hgvsc: ENST00000566653.1:n.550G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.454G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.540G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.344+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.456G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.853G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.344+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+28G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+28G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

16-2256688-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256688
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256688
    reference: chr 16
allele count: 1
allele frequency: 8.735455466648032e-6
allele num: 114476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.540G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.344+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.456G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000566653
  gene symbol: MLST8
  hgvsc: ENST00000566653.1:n.550G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.454G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.344+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.853G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+28G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+28G>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

16-2256696-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256696
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256696
    reference: chr 16
allele count: 1
allele frequency: 8.897113776290972e-6
allele num: 112396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.464G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.344+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000566653
  gene symbol: MLST8
  hgvsc: ENST00000566653.1:n.558G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.861G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.344+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+36G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.462G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+36G>C
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-2256700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256700
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256700
    reference: chr 16
allele count: 1
allele frequency: 9.060925664165851e-6
allele num: 110364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.344+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.865G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.466G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.468G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000566653
  gene symbol: MLST8
  hgvsc: ENST00000566653.1:n.562G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.552G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+40G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+40G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

16-2256705-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256705
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256705
    reference: chr 16
allele count: 3
allele frequency: 2.753657775411672e-5
allele num: 108946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.473C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.870C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000566653
  gene symbol: MLST8
  hgvsc: ENST00000566653.1:n.567C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.471C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.345-39C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.557C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+45C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.345-39C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

16-2256707-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256707
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256707
    reference: chr 16
allele count: 3
allele frequency: 2.769980794799823e-5
allele num: 108304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.345-37C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000566653
  gene symbol: MLST8
  hgvsc: ENST00000566653.1:n.569C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.473C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.345-37C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.872C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.475C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+47C>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+47C>G
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-2256711-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256711
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256711
    reference: chr 16
allele count: 2
allele frequency: 1.88118439369427e-5
allele num: 106316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.876G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.477G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.563G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.479G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.345-33G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000566653
  gene symbol: MLST8
  hgvsc: ENST00000566653.1:n.573G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+51G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.345-33G>C
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-2256721-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256721
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256721
    reference: chr 16
allele count: 1
allele frequency: 1.006461482719056e-5
allele num: 99358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.489T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.573T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.487T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.345-23T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000566653
  gene symbol: MLST8
  hgvsc: ENST00000566653.1:n.583T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+61T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.886T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.345-23T>C
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

16-2256724-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256724
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256724
    reference: chr 16
allele count: 8
allele frequency: 8.192859922577473e-5
allele num: 97646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.492G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.490G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565269
  gene symbol: MLST8
  hgvsc: ENST00000565269.1:n.576G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.889G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.345-20G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.345-20G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+64G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+64G>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

16-2256726-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256726
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256726
    reference: chr 16
allele count: 1
allele frequency: 1.049648367796788e-5
allele num: 95270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.345-18T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.345-18T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.492T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.891T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.494T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+66T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+66T>C
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD

16-2256734-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256734
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256734
    reference: chr 16
allele count: 1
allele frequency: 1.13587314568709e-5
allele num: 88038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.345-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.502C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.899C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.345-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.500C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+74C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+74C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

16-2256737-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256737
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256737
    reference: chr 16
allele count: 1
allele frequency: 1.184216759035574e-5
allele num: 84444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.345-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.505C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.345-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.503C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+77C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+77C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.345-7C>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD

16-2256740-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256740
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256740
    reference: chr 16
allele count: 1
allele frequency: 1.21056581846355e-5
allele num: 82606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.345-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.506G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.508G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.345-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.905G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+80G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+80G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.345-4G>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

16-2256740-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256740
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256740
    reference: chr 16
allele count: 2
allele frequency: 2.4211316369271e-5
allele num: 82606
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.345-4G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.345-4G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.905G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.506G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.508G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+80G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+80G>C
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.345-4G>C
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

16-2256751-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256751
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256751
    reference: chr 16
allele count: 2
allele frequency: 2.754213947339429e-5
allele num: 72616
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.519G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.916G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+91G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+91G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/16-2256754-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256754
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256754
    reference: chr 16
allele count: 1
allele frequency: 1.434432108328313e-5
allele num: 69714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.522A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.520A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*4A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*4A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+94A>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.919A>C
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

16-2256762-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256762
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256763
    reference: chr 16
allele count: 1
allele frequency: 1.654423929587718e-5
allele num: 60444
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*14dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.530dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.532dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.929dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*14dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+104dupC
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+104dupC
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

16-2256763-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256763
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256763
    reference: chr 16
allele count: 3
allele frequency: 5.054078641463661e-5
allele num: 59358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.529C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.531C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.928C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*13C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*13C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+103C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+103C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP

16-2256766-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256766
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256766
    reference: chr 16
allele count: 1
allele frequency: 1.753709094735365e-5
allele num: 57022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*16G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.534G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.931G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.532G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*16G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+106G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+106G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

16-2256767-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256767
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256767
    reference: chr 16
allele count: 2
allele frequency: 3.577049649449134e-5
allele num: 55912
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*17T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.535T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*17T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+107T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.932T>C
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

16-2256771-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256771
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256771
    reference: chr 16
allele count: 6
allele frequency: 1.15977886882901e-4
allele num: 51734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.936C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000567928
  gene symbol: MLST8
  hgvsc: ENST00000567928.1:n.537C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.539C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+111C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*21C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

16-2256774-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256774
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256774
    reference: chr 16
allele count: 1
allele frequency: 2.025931928687196e-5
allele num: 49360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.542C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.939C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*24C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*24C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+114C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+114C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-2256780-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256780
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256780
    reference: chr 16
allele count: 11
allele frequency: 2.495349575790572e-4
allele num: 44082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.945G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.548G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*30G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*30G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+120G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+120G>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

16-2256785-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256785
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256785
    reference: chr 16
allele count: 2
allele frequency: 4.884959210590592e-5
allele num: 40942
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*35A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.553A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.950A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*35A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+125A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+125A>G
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

16-2256787-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256787
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256787
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 39532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.952G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*37G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+127G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.555G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-2256788-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256788
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256788
    reference: chr 16
allele count: 5
allele frequency: 1.270454314462852e-4
allele num: 39356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.556T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*38T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*38T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+128T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+128T>C
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD

16-2256794-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256794
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256794
    reference: chr 16
allele count: 1
allele frequency: 2.86286859433152e-5
allele num: 34930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.959C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.562C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*44C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*44C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+134C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+134C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS

16-2256797-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256797
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256797
    reference: chr 16
allele count: 2
allele frequency: 6.040471156750227e-5
allele num: 33110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.962G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*47G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.565G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*47G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+137G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+137G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

16-2256809-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256809
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256809
    reference: chr 16
allele count: 6
allele frequency: 2.062706270627063e-4
allele num: 29088
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.577T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*59T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*59T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.974T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+149T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+149T>C
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum

16-2256821-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256821
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256821
    reference: chr 16
allele count: 45
allele frequency: 1.81407723937757e-3
allele num: 24806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.589G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.344+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.362+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.986G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*71G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.341+161G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*71G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+161G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-2256821-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256821
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256821
    reference: chr 16
allele count: 1
allele frequency: 4.031282754172378e-5
allele num: 24806
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.344+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*138+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.986G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.589G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.362+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*71G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+161G>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*71G>C
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

16-2256821-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256821
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256821
    reference: chr 16
allele count: 3
allele frequency: 1.209384826251713e-4
allele num: 24806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.431+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.344+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.344+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.208+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*138+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.401+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.142+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.712+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*138+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.545+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.344+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564294
  gene symbol: MLST8
  hgvsc: ENST00000564294.1:n.986G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.401+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.344+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.344+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.398+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*71G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.959+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564679
  gene symbol: MLST8
  hgvsc: ENST00000564679.1:n.589G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*138+161G>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.344+161G>T
  variant of: http://identifiers.org/hgnc/24825
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

16-2256987-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256987
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256987
    reference: chr 16
allele count: 10
allele frequency: 8.574123295892996e-5
allele num: 116630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-207G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.713-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-49G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-49G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/16-2256991-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256991
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256991
    reference: chr 16
allele count: 1
allele frequency: 8.5794196880523e-6
allele num: 116558
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-203C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.432-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-45C>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-45C>A
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

16-2256995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2256995
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2256995
    reference: chr 16
allele count: 1
allele frequency: 8.5794196880523e-6
allele num: 116558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.713-41C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-41C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-2257007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257007
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257007
    reference: chr 16
allele count: 1
allele frequency: 8.566190957528826e-6
allele num: 116738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-187G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-29G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.432-29G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

16-2257009-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257009
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257009
    reference: chr 16
allele count: 1
allele frequency: 8.568246080027418e-6
allele num: 116710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-185C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.432-27C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-27C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

16-2257013-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257013
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257013
    reference: chr 16
allele count: 1
allele frequency: 8.559005785887911e-6
allele num: 116836
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-23A>G
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-23A>G
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

16-2257014-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257014
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257014
    reference: chr 16
allele count: 1
allele frequency: 8.559445347941453e-6
allele num: 116830
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-22T>C
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-180T>C
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff

16-2257015-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257015
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257015
    reference: chr 16
allele count: 1
allele frequency: 8.557101538566857e-6
allele num: 116862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-179G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-21G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.713-21G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum

16-2257018-C-CCCCGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257018
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257023
    reference: chr 16
allele count: 2
allele frequency: 1.712798026856673e-5
allele num: 116768
alternate allele: CCCCGG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-8_960-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-8_342-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.713-8_713-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-8_345-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-8_143-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-8_345-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-8_*139-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-8_402-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-8_345-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-8_345-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-8_209-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-8_*181-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-8_402-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.432-8_432-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-8_*139-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-8_345-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-8_363-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-8_363-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-166_345-162dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-8_345-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-8_*139-4dupGCCCG
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS

16-2257019-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257019
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257019
    reference: chr 16
allele count: 1
allele frequency: 8.587081594449311e-6
allele num: 116454
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.432-17C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-17C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

16-2257021-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257021
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257021
    reference: chr 16
allele count: 4
allele frequency: 3.431002538941879e-5
allele num: 116584
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-173C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.713-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.432-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-15C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-15C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

16-2257022-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257022
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257022
    reference: chr 16
allele count: 1
allele frequency: 8.565310492505354e-6
allele num: 116750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.432-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-14G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-14G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

16-2257025-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257025
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257025
    reference: chr 16
allele count: 2
allele frequency: 1.71124458818899e-5
allele num: 116874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.713-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.432-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-11C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-11C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-2257026-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257026
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257026
    reference: chr 16
allele count: 10
allele frequency: 8.552856654122477e-5
allele num: 116920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.713-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456944
  ensembl transcript: ENST00000562352
  gene symbol: MLST8
  hgvsc: ENST00000562352.1:c.363-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.432-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-168C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-10C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-10C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

16-2257029-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257029
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257029
    reference: chr 16
allele count: 1
allele frequency: 8.537376634907625e-6
allele num: 117132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.713-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-165C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-7C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-7C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.345-7C>T
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

16-2257031-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257031
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257031
    reference: chr 16
allele count: 125
allele frequency: 1.065789024930937e-3
allele num: 117284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000569848
  gene symbol: MLST8
  hgvsc: ENST00000569848.1:n.143-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.345-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*181-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568194
  gene symbol: MLST8
  hgvsc: ENST00000568194.1:n.960-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.399-5C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.713-5C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.345-5C>T
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

16-2257032-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257032
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257032
    reference: chr 16
allele count: 12
allele frequency: 1.022808632504858e-4
allele num: 117324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*181-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.345-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.345-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.345-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000563067
  gene symbol: MLST8
  hgvsc: ENST00000563067.1:n.402-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456063
  ensembl transcript: ENST00000562851
  gene symbol: MLST8
  hgvsc: ENST00000562851.1:c.*139-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.209-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.342-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.345-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.546-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000459612
  ensembl transcript: ENST00000567282
  gene symbol: MLST8
  hgvsc: ENST00000567282.1:c.*139-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*139-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.345-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.713-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*139-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.402-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.363-4G>A
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000380313
  ensembl transcript: ENST00000397124
  gene symbol: MLST8
  hgvsc: ENST00000397124.1:c.345-4G>A
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.345-4G>A
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

16-2257040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2257040
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 2257040
    reference: chr 16
allele count: 1
allele frequency: 8.48824378236143e-6
allele num: 117810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456076
  ensembl transcript: ENST00000565717
  gene symbol: MLST8
  hgvsc: ENST00000565717.1:c.*143C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301724
  ensembl transcript: ENST00000301724
  gene symbol: MLST8
  hgvsc: ENST00000301724.10:c.349C>T
  hgvsp: ENSP00000301724.10:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455046
  ensembl transcript: ENST00000565250
  gene symbol: MLST8
  hgvsc: ENST00000565250.1:c.349C>T
  hgvsp: ENSP00000455046.1:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000561651
  gene symbol: MLST8
  hgvsc: ENST00000561651.1:n.436C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455475
  ensembl transcript: ENST00000563107
  gene symbol: MLST8
  hgvsc: ENST00000563107.1:c.345-154C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456046
  ensembl transcript: ENST00000562479
  gene symbol: MLST8
  hgvsc: ENST00000562479.1:c.367C>T
  hgvsp: ENSP00000456046.1:p.Arg123Trp
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000301725
  ensembl transcript: ENST00000301725
  gene symbol: MLST8
  hgvsc: ENST00000301725.7:c.406C>T
  hgvsp: ENSP00000301725.7:p.Arg136Trp
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000371888
  ensembl transcript: ENST00000382450
  gene symbol: MLST8
  hgvsc: ENST00000382450.4:c.346C>T
  hgvsp: ENSP00000371888.4:p.Arg116Trp
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455458
  ensembl transcript: ENST00000566835
  gene symbol: MLST8
  hgvsc: ENST00000566835.1:c.349C>T
  hgvsp: ENSP00000455458.1:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000562844
  gene symbol: MLST8
  hgvsc: ENST00000562844.1:n.403C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000456405
  ensembl transcript: ENST00000569417
  gene symbol: MLST8
  hgvsc: ENST00000569417.1:c.349C>T
  hgvsp: ENSP00000456405.1:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000455850
  ensembl transcript: ENST00000567623
  gene symbol: MLST8
  hgvsc: ENST00000567623.2:c.*185C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000457870
  ensembl transcript: ENST00000564088
  gene symbol: MLST8
  hgvsc: ENST00000564088.1:c.349C>T
  hgvsp: ENSP00000457870.1:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454698
  ensembl transcript: ENST00000569457
  gene symbol: MLST8
  hgvsc: ENST00000569457.1:c.349C>T
  hgvsp: ENSP00000454698.1:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000565330
  gene symbol: MLST8
  hgvsc: ENST00000565330.1:n.550C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454629
  ensembl transcript: ENST00000570224
  gene symbol: MLST8
  hgvsc: ENST00000570224.1:c.*143C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167965
  ensembl protein: ENSP00000454235
  ensembl transcript: ENST00000565687
  gene symbol: MLST8
  hgvsc: ENST00000565687.1:c.*185C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000568542
  gene symbol: MLST8
  hgvsc: ENST00000568542.1:n.717C>T
  variant of: http://identifiers.org/hgnc/24825
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000167965
  ensembl transcript: ENST00000564319
  gene symbol: MLST8
  hgvsc: ENST00000564319.1:n.213C>T
  variant of: http://identifiers.org/hgnc/24825
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg117Trp
num of homozygotes: 0
reference allele: C

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+8G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+8G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000567928
gene symbol: MLST8
hgvsc: ENST00000567928.1:n.434G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+8G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564679
gene symbol: MLST8
hgvsc: ENST00000564679.1:n.436G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564294
gene symbol: MLST8
hgvsc: ENST00000564294.1:n.833G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+8G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+8G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+8G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+8G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.344+8G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454235
ensembl transcript: ENST00000565687
gene symbol: MLST8
hgvsc: ENST00000565687.1:c.344+8G>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 26
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1285
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 869
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 27644
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 272
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1698
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8614
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 860
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 468
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3739
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14370
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1881
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8902
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1885
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2180
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42172
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.077549532028686e-5
allele num: 16454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64978
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.108e0

QD
type: SiteQuality
SIO_000300: 1.358e1

DP
type: SiteQuality
SIO_000300: 1.706316e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

FS
type: SiteQuality
SIO_000300: 4.677e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.716e0

MQRankSum
type: SiteQuality
SIO_000300: 4.87e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000566653
gene symbol: MLST8
hgvsc: ENST00000566653.1:n.541G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+19G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+19G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+19G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+19G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+19G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+19G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+19G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+19G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+19G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+19G>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 27165
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 836
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 266
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13960
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3518
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1253
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1655
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 560
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 762
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1628
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8463
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41140
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8644
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.120322652924042e-4
allele num: 8926
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63724
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.742e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-2

MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
SIO_000300: 7.67e-1

QD
type: SiteQuality
SIO_000300: 1.169e1

FS
type: SiteQuality
SIO_000300: 6.024e0

DP
type: SiteQuality
SIO_000300: 1.673697e6

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+27dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+27dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+27dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+27dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+27dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+27dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+27dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+27dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+27dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+27dupC
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 9
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1525
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 570
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13794
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27061
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3398
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 966
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8404
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1500
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 782
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1772
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 126
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2657
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1727
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40900
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.587100050787201e-5
allele num: 63008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.055e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

DP
type: SiteQuality
SIO_000300: 1.654819e6

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.151e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+26C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+26C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+26C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+26C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+26C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000566653
gene symbol: MLST8
hgvsc: ENST00000566653.1:n.548C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+26C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+26C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564679
gene symbol: MLST8
hgvsc: ENST00000564679.1:n.454C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+26C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+26C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 1498
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1027
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13749
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 556
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27023
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8405
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1549
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3361
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1829
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 775
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 334
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2778
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40813
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.294630564479119e-4
allele num: 8716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.91e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.28e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.038e0

VQSLOD
type: SiteQuality
SIO_000300: -4.86e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

DP
type: SiteQuality
SIO_000300: 1.650241e6

FS
type: SiteQuality
SIO_000300: 8.955e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000566653
gene symbol: MLST8
hgvsc: ENST00000566653.1:n.549C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000459612
ensembl transcript: ENST00000567282
gene symbol: MLST8
hgvsc: ENST00000567282.1:c.*138+27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+27C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 26966
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1877
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1089
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 583
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1621
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 768
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3317
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8401
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1468
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13682
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2018
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8378
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2840
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40582
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 8.827683615819209e-5
allele num: 11328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8684
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

FS
type: SiteQuality
SIO_000300: 1.075e0

MQRankSum
type: SiteQuality
SIO_000300: -6.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

DP
type: SiteQuality
SIO_000300: 1.644535e6

QD
type: SiteQuality
SIO_000300: 1.622e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.344+28G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+28G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+28G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455458
ensembl transcript: ENST00000566835
gene symbol: MLST8
hgvsc: ENST00000566835.1:c.344+28G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+28G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+28G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+28G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+28G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+28G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+28G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 26939
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 581
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1932
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1146
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13614
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3265
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 8406
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 757
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1441
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 229
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 123
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40497
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2019
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8366
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.531696980399082e-4
allele num: 11326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.895e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

QD
type: SiteQuality
SIO_000300: 1.439e1

DP
type: SiteQuality
SIO_000300: 1.638713e6

VQSLOD
type: SiteQuality
SIO_000300: -4.81e-2

FS
type: SiteQuality
SIO_000300: 1.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.432e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQRankSum
type: SiteQuality
SIO_000300: -3.25e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+28G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+28G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+28G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+28G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+28G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+28G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+28G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+28G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+28G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+28G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+28G>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 229
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8406
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 757
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 581
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1932
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 124
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1146
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1441
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 26939
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3265
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13614
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2980
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8366
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40497
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2019
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.10798924993892e-5
allele num: 16372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.432e0

MQ
type: SiteQuality
SIO_000300: 5.895e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: -3.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.81e-2

DP
type: SiteQuality
SIO_000300: 1.638713e6

QD
type: SiteQuality
SIO_000300: 1.439e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+36G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+36G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+36G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+36G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+36G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+36G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+36G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+36G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+36G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+36G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565269
gene symbol: MLST8
hgvsc: ENST00000565269.1:n.548G>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 513
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8547
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13362
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1570
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2243
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2756
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2259
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 564
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27023
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1002
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 355
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40409
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3718
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1372
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.634360801490537e-5
allele num: 61186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8216
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.709e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.588578e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

QD
type: SiteQuality
SIO_000300: 1.5e1

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.05e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+40G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+40G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+40G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+40G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454235
ensembl transcript: ENST00000565687
gene symbol: MLST8
hgvsc: ENST00000565687.1:c.344+40G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.208+40G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+40G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+40G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+40G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+40G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 2639
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1837
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12646
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26802
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2860
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 654
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8693
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 452
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 889
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2359
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7368
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1885
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4514
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39429
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59882
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8054
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.165228113440197e-5
allele num: 16220
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

DP
type: SiteQuality
SIO_000300: 1.550249e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.445e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.649e0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

QD
type: SiteQuality
SIO_000300: 2.2e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+45C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000459612
ensembl transcript: ENST00000567282
gene symbol: MLST8
hgvsc: ENST00000567282.1:c.*138+45C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+45C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+45C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+45C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+45C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+45C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+45C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.208+45C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+45C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+45C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 803
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8751
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 727
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26426
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2198
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3368
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12137
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2023
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 381
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3056
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38679
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5421
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2091
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7093
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.079752108097125e-5
allele num: 59058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5930
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7912
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

FS
type: SiteQuality
SIO_000300: 3.034e0

QD
type: SiteQuality
SIO_000300: 1.531e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.937e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

DP
type: SiteQuality
SIO_000300: 1.519903e6

MQRankSum
type: SiteQuality
SIO_000300: 6.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.820000000000001e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565269
gene symbol: MLST8
hgvsc: ENST00000565269.1:n.559C>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+47C>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+47C>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.208+47C>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+47C>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+47C>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+47C>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+47C>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+47C>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.344+47C>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+47C>G
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 776
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 9
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 780
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3237
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11940
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 343
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2150
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8763
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2140
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3553
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26189
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7008
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2211
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38380
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5713
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8026
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.111603339580849e-5
allele num: 58690
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11018
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 1.479e1

FS
type: SiteQuality
SIO_000300: 3.031e0

DP
type: SiteQuality
SIO_000300: 1.506402e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.21e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: 5.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.287e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+51G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+51G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+51G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+51G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+51G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+51G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.208+51G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+51G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+51G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+51G>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 9
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25435
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4344
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 629
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1955
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8783
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 949
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11211
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3968
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2299
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7131
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2353
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6749
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 216
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.472342789680197e-5
allele num: 57598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.463431e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

QD
type: SiteQuality
SIO_000300: 1.644e1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+61T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.344+61T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+61T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+61T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+61T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+61T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+61T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+61T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+61T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+61T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+61T>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 2751
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7179
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8451
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 405
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8907
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22263
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1197
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6852
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1675
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2775
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5030
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 136
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31569
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12355
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5054
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9918
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.435834727764191e-5
allele num: 15538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53810
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.161e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.590000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.71e-1

DP
type: SiteQuality
SIO_000300: 1.31257e6

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+64G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+64G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+64G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+64G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+64G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+64G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+64G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+64G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+64G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+64G>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2848
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7914
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1053
bin: 3.75e1
variant carriers: 3

GenotypeDepth
all individuals: 7767
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7751
bin: 1.25e1
variant carriers: 4

GenotypeDepth
all individuals: 1850
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8826
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21333
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2893
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 317
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13855
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4849
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1003
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1201
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30461
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 377
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 1.158748551564311e-3
allele num: 6904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4940
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15430
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

DP
type: SiteQuality
SIO_000300: 1.274224e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

FS
type: SiteQuality
SIO_000300: 3.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

QD
type: SiteQuality
SIO_000300: 1.405e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.34e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+66T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+66T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454629
ensembl transcript: ENST00000570224
gene symbol: MLST8
hgvsc: ENST00000570224.1:c.*138+66T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+66T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+66T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+66T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+66T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.208+66T>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 7037
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8680
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8860
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2083
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19935
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 917
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8863
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 329
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2978
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 131
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28328
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15593
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 337
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4278
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4778
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.433897332950961e-4
allele num: 6974
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6712
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.599e0

MQRankSum
type: SiteQuality
SIO_000300: -2.693e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.31e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

DP
type: SiteQuality
SIO_000300: 1.227354e6

FS
type: SiteQuality
SIO_000300: 2.935e0

VQSLOD
type: SiteQuality
SIO_000300: -2.764e0

QD
type: SiteQuality
SIO_000300: 1.979e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+74C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+74C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.208+74C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+74C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+74C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455458
ensembl transcript: ENST00000566835
gene symbol: MLST8
hgvsc: ENST00000566835.1:c.344+74C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+74C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+74C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+74C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 3416
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5070
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12124
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11755
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2621
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7790
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 682
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15956
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22380
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20848
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3548
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1848
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3509
bin: 7.5e0
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.101370093300832e-5
allele num: 47588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14738
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-2

FS
type: SiteQuality
SIO_000300: 4.425e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.318e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.47e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.34e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
type: SiteQuality
SIO_000300: 1.093382e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+77C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+77C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+77C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+77C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+77C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+77C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564294
gene symbol: MLST8
hgvsc: ENST00000564294.1:n.902C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+77C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+77C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 605
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13448
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13041
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7395
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14054
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3680
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2882
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4277
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 387
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3781
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22948
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19458
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2058
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4034
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.915629322268326e-5
allele num: 14460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5894
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.354e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.548e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.15e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.075e0

DP
type: SiteQuality
SIO_000300: 1.033758e6

QD
type: SiteQuality
SIO_000300: 9.15e0

MQ
type: SiteQuality
SIO_000300: 5.829e1

VQSLOD
type: SiteQuality
SIO_000300: -3.462e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+80G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+80G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+80G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+80G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+80G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+80G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+80G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+80G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+80G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 7195
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13889
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2911
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3935
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3788
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14147
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12984
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24285
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 100
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4018
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1877
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3928
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.242554718335128e-5
allele num: 44592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.97431e5

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.24e-2

QD
type: SiteQuality
SIO_000300: 1.161e1

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.46e-1

FS
type: SiteQuality
SIO_000300: 4.595e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.934e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.013e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+80G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+80G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455458
ensembl transcript: ENST00000566835
gene symbol: MLST8
hgvsc: ENST00000566835.1:c.344+80G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+80G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+80G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+80G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+80G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+80G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+80G>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 7195
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12984
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2911
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 205
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3935
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13889
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3788
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 546
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14147
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1877
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24285
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4018
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18234
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 241
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3928
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7536
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.397233477714126e-4
allele num: 14314
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.161e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.934e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.24e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

FS
type: SiteQuality
SIO_000300: 4.595e0

VQSLOD
type: SiteQuality
SIO_000300: 4.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.013e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

DP
type: SiteQuality
SIO_000300: 9.97431e5

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.344+91G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+91G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455850
ensembl transcript: ENST00000567623
gene symbol: MLST8
hgvsc: ENST00000567623.2:c.*1G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+91G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+91G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+91G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+91G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+91G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000567928
gene symbol: MLST8
hgvsc: ENST00000567928.1:n.517G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2376
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8904
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16226
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2738
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 5363
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 432
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17291
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5981
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2494
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28671
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 253
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1920
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13538
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5547
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.146415521589213e-5
allele num: 38862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5004
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13542
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.59574e5

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.45e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.215e0

FS
type: SiteQuality
SIO_000300: 1.643e0

QD
type: SiteQuality
SIO_000300: 1.044e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.783e0

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+94A>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+94A>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+94A>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+94A>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+94A>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+94A>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+94A>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+94A>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.344+94A>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16536
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5450
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5948
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 418
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2671
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8026
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18057
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2178
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6153
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2549
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1931
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1839
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12242
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29411
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.682835220260772e-5
allele num: 37274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.599e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.55e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

MQRankSum
type: SiteQuality
SIO_000300: 6.74e-1

DP
type: SiteQuality
SIO_000300: 8.2673e5

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455458
ensembl transcript: ENST00000566835
gene symbol: MLST8
hgvsc: ENST00000566835.1:c.344+104dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+104dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.208+104dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454629
ensembl transcript: ENST00000570224
gene symbol: MLST8
hgvsc: ENST00000570224.1:c.*138+104dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+104dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+104dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+104dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+104dupC
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+104dupC
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 388
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20001
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2418
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8275
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1648
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16879
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3989
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5513
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8607
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8340
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30081
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2635
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3934
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31934
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4794
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.895152376440866e-5
allele num: 12666
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.11e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.923e-1

DP
type: SiteQuality
SIO_000300: 7.28163e5

QD
type: SiteQuality
SIO_000300: 3.74e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+103C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+103C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+103C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+103C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+103C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+103C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+103C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+103C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2393
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 383
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8563
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5276
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3906
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 16779
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1597
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20187
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29979
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1949
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8893
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7997
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 181
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 811
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1028
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2538
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.95291872117067e-5
allele num: 12574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4006
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.382435537401073e-5
allele num: 31336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3824
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.16e-2

QD
type: SiteQuality
SIO_000300: 1.183e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

FS
type: SiteQuality
SIO_000300: 5.077e0

DP
type: SiteQuality
SIO_000300: 7.18605e5

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+106G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+106G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+106G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+106G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.344+106G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+106G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+106G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+106G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+106G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 2160
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4881
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16323
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9286
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 20784
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3770
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1485
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 367
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2576
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1095
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9618
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30205
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1877
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7665
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.322340919647004e-4
allele num: 4306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2406
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.045e1

VQSLOD
type: SiteQuality
SIO_000300: -3.655e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.387e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.905e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.27e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

DP
type: SiteQuality
SIO_000300: 6.97731e5

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+107T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+107T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+107T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+107T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000567928
gene symbol: MLST8
hgvsc: ENST00000567928.1:n.533T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+107T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+107T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.344+107T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+107T>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 163
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9643
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3655
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1437
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4682
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2102
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20942
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16207
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29974
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9983
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2574
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 380
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7330
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1248
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29492
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 5.324813631522897e-4
allele num: 3756
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e0

FS
type: SiteQuality
SIO_000300: 2.519e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.447e1

DP
type: SiteQuality
SIO_000300: 6.87925e5

VQSLOD
type: SiteQuality
SIO_000300: 5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.33e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.749e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+111C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+111C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+111C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+111C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+111C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+111C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+111C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+111C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+111C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 1317
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10995
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 21385
bin: 7.5e0
variant carriers: 3

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4029
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1914
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15618
bin: 1.25e1
variant carriers: 5

GenotypeDepth
all individuals: 3301
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 361
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1803
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1823
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 29262
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 174
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11392
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6358
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2507
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11978
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3412
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2056
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 2.208805772345752e-4
allele num: 27164
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.36e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.257e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

DP
type: SiteQuality
SIO_000300: 6.54703e5

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+114C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+114C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+114C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+114C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+114C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+114C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000567928
gene symbol: MLST8
hgvsc: ENST00000567928.1:n.540C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+114C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.208+114C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 3156
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21786
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11937
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3779
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 353
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14966
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1250
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1649
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6125
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2397
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12380
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.858024691358025e-5
allele num: 25920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3238
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.35447e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.83e-1

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -2.085e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.073e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-2

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+120G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+120G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+120G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455458
ensembl transcript: ENST00000566835
gene symbol: MLST8
hgvsc: ENST00000566835.1:c.344+120G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+120G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+120G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+120G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+120G>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 21329
bin: 7.5e0
variant carriers: 4

GenotypeDepth
all individuals: 1513
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1182
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3149
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14731
bin: 2.5e0
variant carriers: 2

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13887
bin: 1.25e1
variant carriers: 8

GenotypeDepth
all individuals: 2431
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 349
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26130
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 615
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4918
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1953
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1750
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2382
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 91
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 89
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2295
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22892
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 3.865073787772312e-3
allele num: 2846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.196e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.25e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

DP
type: SiteQuality
SIO_000300: 5.88038e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.267e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455458
ensembl transcript: ENST00000566835
gene symbol: MLST8
hgvsc: ENST00000566835.1:c.344+125A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+125A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454629
ensembl transcript: ENST00000570224
gene symbol: MLST8
hgvsc: ENST00000570224.1:c.*138+125A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+125A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+125A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+125A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+125A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+125A>G
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 1373
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16391
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12862
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2887
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21181
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2181
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 158
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1146
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 349
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2261
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24391
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2570
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 602
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16774
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4525
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11130
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2164
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 9.293680297397769e-4
allele num: 2152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1394
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.56e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.62779e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.915e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.097e0

QD
type: SiteQuality
SIO_000300: 1.412e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+127G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+127G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+127G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+127G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+127G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.142+127G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+127G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+127G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 1358
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21152
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17016
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2804
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12356
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1148
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2081
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4375
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2739
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17277
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2469
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1724
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23453
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 320
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20380
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

FS
type: SiteQuality
SIO_000300: 3.136e0

DP
type: SiteQuality
SIO_000300: 5.53155e5

VQSLOD
type: SiteQuality
SIO_000300: -4.343e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.67e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+128T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+128T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.344+128T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564294
gene symbol: MLST8
hgvsc: ENST00000564294.1:n.953T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.208+128T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455458
ensembl transcript: ENST00000566835
gene symbol: MLST8
hgvsc: ENST00000566835.1:c.344+128T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+128T>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 2081
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2799
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17055
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1316
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 21205
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 61
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 12311
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1147
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2459
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23772
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2199
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17382
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2389
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 579
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4424
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 5
allele frequency: 4.551247041689423e-4
allele num: 10986
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2044
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20286
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1974
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.668e0

DP
type: SiteQuality
SIO_000300: 5.52464e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.67e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.153e0

QD
type: SiteQuality
SIO_000300: 1.31e1

VQSLOD
type: SiteQuality
SIO_000300: -1.43e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+134C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454629
ensembl transcript: ENST00000570224
gene symbol: MLST8
hgvsc: ENST00000570224.1:c.*138+134C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+134C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+134C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+134C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+134C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+134C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.344+134C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 158
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18930
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21300
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 2600
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10632
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1157
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1891
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1111
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21541
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2873
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19014
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2688
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4051
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 178
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2126
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 6.031363088057901e-4
allele num: 1658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1048
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.24094e5

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.341e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.04e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

VQSLOD
type: SiteQuality
SIO_000300: 3.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 1.232e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+137G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+137G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+137G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+137G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+137G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+137G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+137G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+137G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19891
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1797
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9851
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2514
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21136
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1143
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1103
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2021
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19847
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3869
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1654
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3314
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3037
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19884
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 165
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1462
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 5.045408678102926e-4
allele num: 1982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.997361161089121e-5
allele num: 16674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 946
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.405e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.09773e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.19e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.974e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.905e0

QD
type: SiteQuality
SIO_000300: 1.097e1

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+149T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+149T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+149T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+149T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+149T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.344+149T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*138+149T>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 1330
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 22001
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 2296
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20619
bin: 7.5e0
variant carriers: 6

GenotypeDepth
all individuals: 8139
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1057
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 344
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1435
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 252
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 4733
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 162
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16079
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3213
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3339
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21578
bin: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14260
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 5.968961400716276e-4
allele num: 10052
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1074
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.164e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 7.162e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-2

DP
type: SiteQuality
SIO_000300: 4.75427e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.714e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*138+161G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.398+161G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+161G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+161G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+161G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.401+161G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.431+161G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+161G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 153
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6189
bin: 1.25e1
variant carriers: 11

GenotypeDepth
all individuals: 1522
bin: 2.25e1
variant carriers: 6

GenotypeDepth
all individuals: 22499
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 1898
bin: 1.75e1
variant carriers: 10

GenotypeDepth
all individuals: 21885
bin: 7.5e0
variant carriers: 13

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 822
bin: 3.25e1
variant carriers: 6

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1706
bin: 2.75e1
variant carriers: 4

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 3.75e1
variant carriers: 7

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4828
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2267
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1791
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3098
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.75e1
variant carriers: 47

GenotypeQuality
all individuals: 21107
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 5820
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12718
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 277
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 89
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 960
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 160
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 325
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.288659793814433e-3
allele num: 776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

South Asian
type: Population
allele count: 33
allele frequency: 3.431780366056572e-3
allele num: 9616
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.536098310291859e-3
allele num: 1302
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 4.716981132075472e-3
allele num: 212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 6.895362868470954e-4
allele num: 11602
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 1.432e0

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

DP
type: SiteQuality
SIO_000300: 4.45446e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

QD
type: SiteQuality
SIO_000300: 1.228e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.066e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.712+161G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.545+161G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+161G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.344+161G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+161G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.959+161G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.401+161G>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.344+161G>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 22499
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1522
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1706
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 822
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1898
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 21885
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 340
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6189
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5820
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1791
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12718
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3098
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4828
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2267
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.619203585588692e-5
allele num: 11602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.066e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 1.432e0

DP
type: SiteQuality
SIO_000300: 4.45446e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

QD
type: SiteQuality
SIO_000300: 1.228e1

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.344+161G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.344+161G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.362+161G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455850
ensembl transcript: ENST00000567623
gene symbol: MLST8
hgvsc: ENST00000567623.2:c.*71G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.341+161G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456046
ensembl transcript: ENST00000562479
gene symbol: MLST8
hgvsc: ENST00000562479.1:c.362+161G>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454629
ensembl transcript: ENST00000570224
gene symbol: MLST8
hgvsc: ENST00000570224.1:c.*138+161G>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 0
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1522
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6189
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21885
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22499
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1706
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 340
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1898
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 822
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4828
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2267
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5820
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12718
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3098
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1302
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.119800332778702e-4
allele num: 9616
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

FS
type: SiteQuality
SIO_000300: 1.432e0

QD
type: SiteQuality
SIO_000300: 1.228e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.066e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.45446e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.342-49G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.345-49G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.345-49G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.432-49G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.960-49G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454235
ensembl transcript: ENST00000565687
gene symbol: MLST8
hgvsc: ENST00000565687.1:c.*181-49G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 570
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2902
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1523
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4482
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 4663
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3770
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2173
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2519
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1768
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3749
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4822
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1618
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2520
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4865
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2056
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5009
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4229
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 444
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 207
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45658
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1102
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.122755519470381e-5
allele num: 64046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.213592233009709e-3
allele num: 6592
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.481535e6

MQRankSum
type: SiteQuality
SIO_000300: -3.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.303e0

FS
type: SiteQuality
SIO_000300: 9.340000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.94e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.209-45C>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.546-45C>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454629
ensembl transcript: ENST00000570224
gene symbol: MLST8
hgvsc: ENST00000570224.1:c.*139-45C>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*139-45C>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.960-45C>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.713-45C>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 4663
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4483
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1802
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2903
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3748
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 574
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1522
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2352
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1634
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2059
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2507
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4823
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4863
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3770
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4229
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5011
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2289
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45657
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 463
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.36213258684311e-5
allele num: 15718
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.134e1

MQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.616e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 2.295e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.85e-1

DP
type: SiteQuality
SIO_000300: 3.482806e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-2

MQ
type: SiteQuality
SIO_000300: 5.883e1

VQSLOD
type: SiteQuality
SIO_000300: -2.892e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*139-41C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.209-41C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.345-199C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455850
ensembl transcript: ENST00000567623
gene symbol: MLST8
hgvsc: ENST00000567623.2:c.*181-41C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.432-41C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 2904
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3749
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2471
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1948
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4863
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4663
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 565
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1878
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2633
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5011
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2062
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1660
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1518
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3770
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4483
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4823
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4229
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45660
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 993
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2818
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 1.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56206067043644e-5
allele num: 64018
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

VQSLOD
type: SiteQuality
SIO_000300: -1.018e0

MQ
type: SiteQuality
SIO_000300: 5.805e1

QD
type: SiteQuality
SIO_000300: 9.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 3.485553e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.083e0

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.345-29G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.960-29G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.713-29G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.345-29G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454629
ensembl transcript: ENST00000570224
gene symbol: MLST8
hgvsc: ENST00000570224.1:c.*139-29G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.209-29G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 1535
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5012
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4822
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1165
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4486
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2100
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1730
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2204
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3771
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2080
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3750
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2906
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4864
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4663
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3405
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4229
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45664
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 699
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1876
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3624
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.516530178950561e-4
allele num: 6594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.495226e6

QD
type: SiteQuality
SIO_000300: 1.168e1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.174e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.522e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.14e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.713-27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.345-27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455850
ensembl transcript: ENST00000567623
gene symbol: MLST8
hgvsc: ENST00000567623.2:c.*181-27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.363-27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301725
ensembl transcript: ENST00000301725
gene symbol: MLST8
hgvsc: ENST00000301725.7:c.402-27C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.342-27C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 3771
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2135
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1090
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4822
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2083
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 491
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1526
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3471
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5012
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1750
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4864
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2172
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4664
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3749
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4487
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2906
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1898
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45664
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 578
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3696
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64068
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.325910931174089e-5
allele num: 15808
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.248e0

DP
type: SiteQuality
SIO_000300: 3.497289e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.124e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

FS
type: SiteQuality
SIO_000300: 3.259e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.42e-1

QD
type: SiteQuality
SIO_000300: 8.17e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.363-23A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.432-23A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.345-181A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.345-23A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.713-23A>G
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.342-23A>G
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1953
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4487
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2283
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2086
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 942
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4864
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1789
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 461
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3669
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3771
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1521
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4664
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3749
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4822
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5012
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1327
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45668
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.298815822625347e-5
allele num: 15876
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.746e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

FS
type: SiteQuality
SIO_000300: 8.401999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.501343e6

QD
type: SiteQuality
SIO_000300: 8.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.595e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.345-22T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.345-22T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.399-22T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.713-22T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.432-22T>C
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455850
ensembl transcript: ENST00000567623
gene symbol: MLST8
hgvsc: ENST00000567623.2:c.*181-22T>C
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 1795
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3748
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 459
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 888
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4487
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3744
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3771
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1522
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5012
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2301
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1911
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4664
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4822
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2086
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4865
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 908
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45668
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4135
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.29643621710112e-5
allele num: 15882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.59e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.05e-1

DP
type: SiteQuality
SIO_000300: 3.502275e6

MQ
type: SiteQuality
SIO_000300: 5.893e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.27e-1

QD
type: SiteQuality
SIO_000300: 1.14e1

FS
type: SiteQuality
SIO_000300: 2.499e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000459612
ensembl transcript: ENST00000567282
gene symbol: MLST8
hgvsc: ENST00000567282.1:c.*139-21G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454698
ensembl transcript: ENST00000569457
gene symbol: MLST8
hgvsc: ENST00000569457.1:c.345-21G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.345-21G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.345-21G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.342-21G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.432-21G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 3819
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5012
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 830
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4488
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2329
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3771
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4665
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1801
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4821
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1521
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 455
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4864
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2087
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1863
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3748
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2907
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45668
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 504
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1821
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558943659776136e-5
allele num: 64146
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.976e0

VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.503391e6

MQRankSum
type: SiteQuality
SIO_000300: -6.65e-1

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.345-8_345-4dupGCCCG
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.399-8_399-4dupGCCCG
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455850
ensembl transcript: ENST00000567623
gene symbol: MLST8
hgvsc: ENST00000567623.2:c.*181-8_*181-4dupGCCCG
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.546-8_546-4dupGCCCG
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*139-8_*139-4dupGCCCG
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 444
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4821
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3862
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4864
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 787
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2414
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1506
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2911
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2966
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2095
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1741
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4488
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3771
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3748
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1837
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4666
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 530
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1316
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4284
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45667
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 188
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560792882784454e-5
allele num: 64070
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15874
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

DP
type: SiteQuality
SIO_000300: 3.506079e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

QD
type: SiteQuality
SIO_000300: 9.609999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -7.676e0

MQ
type: SiteQuality
SIO_000300: 5.177e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

VQSLOD
type: SiteQuality
SIO_000300: -1.664e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 1.5246e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.399-17C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.345-175C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*139-17C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.713-17C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.345-17C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 434
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2475
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2101
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1857
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1846
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 810
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4489
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2925
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4865
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3753
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3766
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1511
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5016
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4666
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2966
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3771
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1286
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45665
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 327
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3877
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 908
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15914
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9172
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566808723990975e-5
allele num: 63824
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 3.135e0

DP
type: SiteQuality
SIO_000300: 3.507396e6

VQSLOD
type: SiteQuality
SIO_000300: -3.404e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.207e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.042e0

MQ
type: SiteQuality
SIO_000300: 5.891e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454235
ensembl transcript: ENST00000565687
gene symbol: MLST8
hgvsc: ENST00000565687.1:c.*181-15C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000459612
ensembl transcript: ENST00000567282
gene symbol: MLST8
hgvsc: ENST00000567282.1:c.*139-15C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.363-15C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455458
ensembl transcript: ENST00000566835
gene symbol: MLST8
hgvsc: ENST00000566835.1:c.345-15C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.345-15C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 1489
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4864
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4488
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1617
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2107
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3771
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4668
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3840
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1885
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 428
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 748
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3752
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2539
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4821
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2921
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4266
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 896
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45673
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 591
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9188
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169864295741694e-4
allele num: 8548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.130086390384375e-5
allele num: 63896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.736e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

QD
type: SiteQuality
SIO_000300: 9.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.52e-1

DP
type: SiteQuality
SIO_000300: 3.509667e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

MQ
type: SiteQuality
SIO_000300: 5.887e1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.345-172G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568542
gene symbol: MLST8
hgvsc: ENST00000568542.1:n.713-14G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455458
ensembl transcript: ENST00000566835
gene symbol: MLST8
hgvsc: ENST00000566835.1:c.345-14G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.209-14G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.399-14G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 4488
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4667
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4864
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2111
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1522
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2626
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1489
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 668
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5013
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3930
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 418
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1896
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3771
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3751
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2918
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4821
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4603
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45672
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9226
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.259389083625437e-5
allele num: 15976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63992
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 4.999e0

DP
type: SiteQuality
SIO_000300: 3.511694e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e-1

QD
type: SiteQuality
SIO_000300: 1.736e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.345-11C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.345-11C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.345-11C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.345-169C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.345-11C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.209-11C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 2967
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4041
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 564
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1981
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4821
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1374
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2734
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4487
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 403
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1459
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4864
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2113
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4668
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3750
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1856
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2921
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5011
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3771
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4782
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1459
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1008
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45682
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64050
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9256
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.24890720619458e-4
allele num: 16014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.219e0

FS
type: SiteQuality
SIO_000300: 1.6902e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

QD
type: SiteQuality
SIO_000300: 1.296e1

DP
type: SiteQuality
SIO_000300: 3.516099e6

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*139-10C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456405
ensembl transcript: ENST00000569417
gene symbol: MLST8
hgvsc: ENST00000569417.1:c.345-10C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.960-10C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456076
ensembl transcript: ENST00000565717
gene symbol: MLST8
hgvsc: ENST00000565717.1:c.*139-10C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454235
ensembl transcript: ENST00000565687
gene symbol: MLST8
hgvsc: ENST00000565687.1:c.*181-10C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 536
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2918
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2011
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4862
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1451
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2968
bin: 8.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2776
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4073
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2120
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 385
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1322
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4821
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1855
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5012
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2405
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3748
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4486
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4669
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 3772
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4854
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45687
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 103
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.494076568150642e-4
allele num: 16038
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.803233660028715e-5
allele num: 64076
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170138076293003e-4
allele num: 8546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.235e-1

QD
type: SiteQuality
SIO_000300: 1.076e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 8.021000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 4.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

DP
type: SiteQuality
SIO_000300: 3.517949e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.345-7C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000565330
gene symbol: MLST8
hgvsc: ENST00000565330.1:n.546-7C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000564319
gene symbol: MLST8
hgvsc: ENST00000564319.1:n.209-7C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.432-7C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455046
ensembl transcript: ENST00000565250
gene symbol: MLST8
hgvsc: ENST00000565250.1:c.345-7C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.345-7C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.143-7C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.363-7C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 3773
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5011
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2081
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4228
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1198
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 364
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3749
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 456
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4181
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4488
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2970
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2865
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4821
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4862
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1412
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4667
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2404
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1855
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2127
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2918
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45691
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 401
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4954
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64172
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.210408644888833e-5
allele num: 16102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.119e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.99e-1

FS
type: SiteQuality
SIO_000300: 1.186e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

VQSLOD
type: SiteQuality
SIO_000300: -3.149e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 3.522067e6

QD
type: SiteQuality
SIO_000300: 1.547e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.432-5C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000371888
ensembl transcript: ENST00000382450
gene symbol: MLST8
hgvsc: ENST00000382450.4:c.342-5C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.363-5C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455850
ensembl transcript: ENST00000567623
gene symbol: MLST8
hgvsc: ENST00000567623.2:c.*181-5C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000301724
ensembl transcript: ENST00000301724
gene symbol: MLST8
hgvsc: ENST00000301724.10:c.345-5C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454629
ensembl transcript: ENST00000570224
gene symbol: MLST8
hgvsc: ENST00000570224.1:c.*139-5C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.345-163C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 351
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1860
bin: 9.25e1
variant carriers: 8

GenotypeDepth
all individuals: 2921
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2966
bin: 8.25e1
variant carriers: 4

GenotypeDepth
all individuals: 4275
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2914
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1382
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5003
bin: 5.75e1
variant carriers: 3

GenotypeDepth
all individuals: 4752
bin: 9.75e1
variant carriers: 96

GenotypeDepth
all individuals: 2132
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 405
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4849
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4214
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1108
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 4472
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3769
bin: 7.75e1
variant carriers: 3

GenotypeDepth
all individuals: 3745
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2104
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2401
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 4810
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1536
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1593
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45708
bin: 9.75e1
variant carriers: 125

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5226
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16156
num of homozygotes: 0

East Asian
type: Population
allele count: 124
allele frequency: 1.4482597523943e-2
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.556420233463035e-5
allele num: 64250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

QD
type: SiteQuality
SIO_000300: 1.179e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.24e0

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

DP
type: SiteQuality
SIO_000300: 3.531398e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000562844
gene symbol: MLST8
hgvsc: ENST00000562844.1:n.399-4G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.363-4G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000454235
ensembl transcript: ENST00000565687
gene symbol: MLST8
hgvsc: ENST00000565687.1:c.*181-4G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.143-4G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000457870
ensembl transcript: ENST00000564088
gene symbol: MLST8
hgvsc: ENST00000564088.1:c.345-4G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000455475
ensembl transcript: ENST00000563107
gene symbol: MLST8
hgvsc: ENST00000563107.1:c.345-162G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000561651
gene symbol: MLST8
hgvsc: ENST00000561651.1:n.432-4G>A
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.960-4G>A
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 4812
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 340
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2969
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5001
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4473
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4730
bin: 9.75e1
variant carriers: 6

GenotypeDepth
all individuals: 2133
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2414
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3746
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4291
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2123
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1082
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4215
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1371
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2957
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2913
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3773
bin: 7.75e1
variant carriers: 2

GenotypeDepth
all individuals: 4850
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1861
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45712
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 362
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1030
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5269
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 10
allele frequency: 1.074806534823732e-3
allele num: 9304
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.183527083848628e-5
allele num: 16172
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

QD
type: SiteQuality
SIO_000300: 1.382e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 4.44e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

DP
type: SiteQuality
SIO_000300: 3.530736e6

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000459612
ensembl transcript: ENST00000567282
gene symbol: MLST8
hgvsc: ENST00000567282.1:c.*143C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000569848
gene symbol: MLST8
hgvsc: ENST00000569848.1:n.147C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456944
ensembl transcript: ENST00000562352
gene symbol: MLST8
hgvsc: ENST00000562352.1:c.367C>T
hgvsp: ENSP00000456944.1:p.Arg123Trp
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000380313
ensembl transcript: ENST00000397124
gene symbol: MLST8
hgvsc: ENST00000397124.1:c.349C>T
hgvsp: ENSP00000380313.1:p.Arg117Trp
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000568194
gene symbol: MLST8
hgvsc: ENST00000568194.1:n.964C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000167965
ensembl transcript: ENST00000563067
gene symbol: MLST8
hgvsc: ENST00000563067.1:n.406C>T
variant of: http://identifiers.org/hgnc/24825

Annotation
canonical: false
consequence: 3_prime_UTR_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000167965
ensembl protein: ENSP00000456063
ensembl transcript: ENST00000562851
gene symbol: MLST8
hgvsc: ENST00000562851.1:c.*143C>T
variant of: http://identifiers.org/hgnc/24825

GenotypeDepth
all individuals: 3746
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2969
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2925
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4813
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2227
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2147
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4665
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3772
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 265
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1240
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4851
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5001
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1861
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4726
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2414
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3121
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 800
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4215
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4473
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45719
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5756
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 8.25e1
variant carriers: 0