8-17503683-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503683
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503683
    reference: chr 8
allele count: 2
allele frequency: 5.85480093676815e-5
allele num: 34160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1348-35C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.378-35C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1963-35C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3438-35C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1035-35C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3600-35C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1098-35C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1341-35C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.816-35C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.298-35C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3438-35C>A
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19307
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

8-17503684-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503684
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503685
    reference: chr 8
allele count: 1804
allele frequency: 1.164622336991608e-1
allele num: 15490
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1348-37dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3600-37dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.378-37dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3438-37dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1963-37dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1341-37dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.816-37dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1035-37dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1098-37dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.298-37dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3438-37dupT
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 2.5e0
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19206
  bin: 1.25e1
  variant carriers: 1251
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 2.25e1
  variant carriers: 179
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 1.75e1
  variant carriers: 422
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20808
  bin: 7.5e0
  variant carriers: 1375
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 2.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 5.75e1
  variant carriers: 239
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

8-17503684-T-TAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503684
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503686
    reference: chr 8
allele count: 24
allele frequency: 1.549386701097482e-3
allele num: 15490
alternate allele: TAA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1035-38_1035-37dupTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.298-38_298-37dupTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3438-38_3438-37dupTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1963-38_1963-37dupTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1098-38_1098-37dupTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3600-38_3600-37dupTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1341-38_1341-37dupTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.816-38_816-37dupTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.378-38_378-37dupTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3438-38_3438-37dupTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1348-38_*1348-37dupTT
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20808
  bin: 7.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 19206
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 2.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

8-17503684-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503684
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503683
    reference: chr 8
allele count: 1831
allele frequency: 1.182052937378954e-1
allele num: 15490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1341-37delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.298-37delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3600-37delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1963-37delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3438-37delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3438-37delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1098-37delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1348-37delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.816-37delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1035-37delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.378-37delT
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 2.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 2.25e1
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19206
  bin: 1.25e1
  variant carriers: 1102
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20808
  bin: 7.5e0
  variant carriers: 792
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 1.75e1
  variant carriers: 546
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 2.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 5.75e1
  variant carriers: 396
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: TA
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

8-17503684-TAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503684
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503682
    reference: chr 8
allele count: 33
allele frequency: 2.130406714009038e-3
allele num: 15490
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19206
  bin: 1.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 20808
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 32692
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8940
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3137
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3734
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 8.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 6.25e1
  variant carriers: 2
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 1
  allele frequency: 7.530120481927711e-4
  allele num: 1328
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 124
  num of homozygotes: 0
population: African
  type: Population
  allele count: 6
  allele frequency: 4.267425320056899e-3
  allele num: 1406
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 5
  allele frequency: 1.995211492418196e-3
  allele num: 2506
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TAA
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

8-17503684-TAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503684
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503681
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 15490
alternate allele: T
canonical: false
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2302
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32692
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3137
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8940
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3734
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 124
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1328
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2506
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1406
  num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: TAAA
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-17503689-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503689
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503689
    reference: chr 8
allele count: 1
allele frequency: 1.997523071391475e-5
allele num: 50062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.298-41T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3600-41T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.378-41T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3438-41T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1035-41T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1348-41T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1341-41T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.816-41T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1963-41T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3438-41T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1098-41T>C
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17050
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4716
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD

8-17503691-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503691
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503691
    reference: chr 8
allele count: 51
allele frequency: 1.032430462771772e-3
allele num: 49398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1341-43T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1348-43T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.378-43T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3600-43T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.298-43T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1963-43T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1098-43T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1035-43T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.816-43T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3438-43T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3438-43T>A
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 24717
  bin: 7.5e0
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16712
  bin: 1.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 9571
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 9.75e1
  variant carriers: 44
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

8-17503697-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503697
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503697
    reference: chr 8
allele count: 5
allele frequency: 1.105754345614578e-4
allele num: 45218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1341-49T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.816-49T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3600-49T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1035-49T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3438-49T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1098-49T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.378-49T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.298-49T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1963-49T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3438-49T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1348-49T>C
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4917
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9457
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15960
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/8-17503699-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503699
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503699
    reference: chr 8
allele count: 1
allele frequency: 2.442598925256473e-5
allele num: 40940
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1341-51G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3600-51G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1963-51G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3438-51G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.298-51G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.816-51G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.378-51G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1348-51G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1035-51G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1098-51G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3438-51G>T
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

8-17503699-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503699
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503699
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 40940
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3438-51G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.298-51G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3600-51G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.816-51G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1348-51G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1098-51G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3438-51G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1963-51G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.378-51G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1341-51G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1035-51G>C
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 15957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9433
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

8-17503700-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17503700
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17503700
    reference: chr 8
allele count: 55
allele frequency: 1.414027149321267e-3
allele num: 38896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1341-52A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1035-52A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.298-52A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3600-52A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.378-52A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1963-52A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1348-52A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3438-52A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1098-52A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3438-52A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.816-52A>G
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15984
  bin: 1.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 25452
  bin: 7.5e0
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9443
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4840
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 4.75e1
  variant carriers: 4
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

8-17504443-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504443
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504443
    reference: chr 8
allele count: 1
allele frequency: 8.448800270361608e-6
allele num: 118360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+48A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+48A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+48A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+48A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+48A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+48A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+48A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+48A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+48A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+48A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+48A>G
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8762
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3478
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

8-17504443-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504443
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504442
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 118360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+47delG
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+47delG
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+47delG
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+47delG
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+47delG
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+47delG
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+47delG
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+47delG
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+47delG
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+47delG
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+47delG
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 13438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3478
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TC
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

8-17504448-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504448
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504448
    reference: chr 8
allele count: 35
allele frequency: 2.947269144618287e-4
allele num: 118754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+43C>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+43C>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+43C>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+43C>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+43C>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+43C>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+43C>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+43C>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+43C>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+43C>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+43C>G
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14216
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9314
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15894
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

8-17504450-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504450
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504450
    reference: chr 8
allele count: 1
allele frequency: 8.413117733169558e-6
allele num: 118862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+41C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+41C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+41C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+41C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+41C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+41C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+41C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+41C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+41C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+41C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+41C>A
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16300
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14512
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

8-17504453-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504453
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504453
    reference: chr 8
allele count: 1083
allele frequency: 9.131996559691047e-3
allele num: 118594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+38G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+38G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+38G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+38G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+38G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+38G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+38G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+38G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+38G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+38G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+38G>A
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 1.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 4.25e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 15040
  bin: 2.75e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 3.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 9905
  bin: 3.25e1
  variant carriers: 216
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16369
  bin: 2.25e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 9.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 3.75e1
  variant carriers: 1
num of homozygotes: 58
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-17504454-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504454
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504454
    reference: chr 8
allele count: 11
allele frequency: 9.254896681698862e-5
allele num: 118856
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+37C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+37C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+37C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+37C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+37C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+37C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+37C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+37C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+37C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+37C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+37C>T
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15602
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16671
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

8-17504457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504457
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504457
    reference: chr 8
allele count: 1
allele frequency: 8.389824820457749e-6
allele num: 119192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+34C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+34C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+34C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+34C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+34C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+34C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+34C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+34C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+34C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+34C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+34C>T
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15963
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

8-17504460-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504460
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504460
    reference: chr 8
allele count: 1
allele frequency: 8.389543273264204e-6
allele num: 119196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+31G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+31G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+31G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+31G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+31G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+31G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+31G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+31G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+31G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+31G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+31G>C
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9140
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

8-17504462-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504462
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504462
    reference: chr 8
allele count: 2
allele frequency: 1.676867611302088e-5
allele num: 119270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+29G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+29G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+29G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+29G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+29G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+29G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+29G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+29G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+29G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+29G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+29G>A
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28251
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP

8-17504463-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504463
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504463
    reference: chr 8
allele count: 6
allele frequency: 5.027989139543459e-5
allele num: 119332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+28C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+28C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+28C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+28C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+28C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+28C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+28C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+28C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+28C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+28C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+28C>T
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11145
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

8-17504467-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504467
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504467
    reference: chr 8
allele count: 4
allele frequency: 3.338173685176839e-5
allele num: 119826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+24C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+24C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+24C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+24C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+24C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+24C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+24C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+24C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+24C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+24C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+24C>T
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3511
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

8-17504467-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504467
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504467
    reference: chr 8
allele count: 2
allele frequency: 1.66908684258842e-5
allele num: 119826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+24C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+24C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+24C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+24C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+24C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+24C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+24C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+24C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+24C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+24C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+24C>A
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18037
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/8-17504469-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504469
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504469
    reference: chr 8
allele count: 2
allele frequency: 1.667027856035474e-5
allele num: 119974
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+22T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+22T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+22T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+22T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+22T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+22T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+22T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+22T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+22T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+22T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+22T>G
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-17504475-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504475
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504475
    reference: chr 8
allele count: 1
allele frequency: 8.322929671244279e-6
allele num: 120150
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+16T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+16T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+16T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+16T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+16T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+16T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+16T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+16T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+16T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+16T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+16T>G
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-17504476-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504476
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504476
    reference: chr 8
allele count: 2
allele frequency: 1.6641427168794e-5
allele num: 120182
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+15G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+15G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+15G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+15G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+15G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+15G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+15G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+15G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+15G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+15G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+15G>C
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18330
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 2.25e1
  variant carriers: 0
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: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

8-17504478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504478
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504478
    reference: chr 8
allele count: 1
allele frequency: 8.316838270762986e-6
allele num: 120238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+13C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+13C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+13C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+13C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+13C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+13C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+13C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+13C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+13C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+13C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+13C>T
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

8-17504480-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504480
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504480
    reference: chr 8
allele count: 4
allele frequency: 3.326292680492956e-5
allele num: 120254
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340+11A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097+11A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034+11A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297+11A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377+11A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599+11A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962+11A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347+11A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437+11A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815+11A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437+11A>C
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11608
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

8-17504491-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504491
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504491
    reference: chr 8
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.815G>C
  hgvsp: ENSP00000382921.1:p.Arg272Thr
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1034G>C
  hgvsp: ENSP00000445738.1:p.Arg345Thr
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3437G>C
  hgvsp: ENSP00000371293.3:p.Arg1146Thr
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1340G>C
  hgvsp: ENSP00000371285.3:p.Arg447Thr
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.297G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3599G>C
  hgvsp: ENSP00000262102.6:p.Arg1200Thr
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.377G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1347G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1097G>C
  hgvsp: ENSP00000297488.6:p.Arg366Thr
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3437G>C
  hgvsp: ENSP00000430167.1:p.Arg1146Thr
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1962G>C
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1200Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

8-17504498-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504498
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504498
    reference: chr 8
allele count: 2
allele frequency: 1.659888787451241e-5
allele num: 120490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.370A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3592A>G
  hgvsp: ENSP00000262102.6:p.Ile1198Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.290A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3430A>G
  hgvsp: ENSP00000371293.3:p.Ile1144Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.808A>G
  hgvsp: ENSP00000382921.1:p.Ile270Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1333A>G
  hgvsp: ENSP00000371285.3:p.Ile445Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1027A>G
  hgvsp: ENSP00000445738.1:p.Ile343Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1090A>G
  hgvsp: ENSP00000297488.6:p.Ile364Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1340A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1955A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3430A>G
  hgvsp: ENSP00000430167.1:p.Ile1144Val
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1198Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

8-17504498-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504498
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504498
    reference: chr 8
allele count: 1
allele frequency: 8.299443937256203e-6
allele num: 120490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.808A>T
  hgvsp: ENSP00000382921.1:p.Ile270Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1333A>T
  hgvsp: ENSP00000371285.3:p.Ile445Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1090A>T
  hgvsp: ENSP00000297488.6:p.Ile364Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1027A>T
  hgvsp: ENSP00000445738.1:p.Ile343Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.370A>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1955A>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.290A>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3430A>T
  hgvsp: ENSP00000430167.1:p.Ile1144Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3430A>T
  hgvsp: ENSP00000371293.3:p.Ile1144Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1340A>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3592A>T
  hgvsp: ENSP00000262102.6:p.Ile1198Phe
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1198Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-17504518-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504518
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504518
    reference: chr 8
allele count: 2
allele frequency: 1.65809981760902e-5
allele num: 120620
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1320G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.788G>T
  hgvsp: ENSP00000382921.1:p.Arg263Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1935G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1313G>T
  hgvsp: ENSP00000371285.3:p.Arg438Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3572G>T
  hgvsp: ENSP00000262102.6:p.Arg1191Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1007G>T
  hgvsp: ENSP00000445738.1:p.Arg336Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1070G>T
  hgvsp: ENSP00000297488.6:p.Arg357Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3410G>T
  hgvsp: ENSP00000371293.3:p.Arg1137Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3410G>T
  hgvsp: ENSP00000430167.1:p.Arg1137Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.350G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.823G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.270G>T
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1191Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ

8-17504519-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504519
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504519
    reference: chr 8
allele count: 1
allele frequency: 8.290224167661493e-6
allele num: 120624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.349C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3409C>T
  hgvsp: ENSP00000430167.1:p.Arg1137Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3571C>T
  hgvsp: ENSP00000262102.6:p.Arg1191Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1006C>T
  hgvsp: ENSP00000445738.1:p.Arg336Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.822C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1319C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1312C>T
  hgvsp: ENSP00000371285.3:p.Arg438Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1934C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3409C>T
  hgvsp: ENSP00000371293.3:p.Arg1137Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.269C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1069C>T
  hgvsp: ENSP00000297488.6:p.Arg357Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.787C>T
  hgvsp: ENSP00000382921.1:p.Arg263Trp
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1191Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-17504521-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504521
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504521
    reference: chr 8
allele count: 1
allele frequency: 8.289674381590291e-6
allele num: 120632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1317C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1004C>T
  hgvsp: ENSP00000445738.1:p.Ala335Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.820C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3569C>T
  hgvsp: ENSP00000262102.6:p.Ala1190Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.267C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3407C>T
  hgvsp: ENSP00000430167.1:p.Ala1136Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.347C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.785C>T
  hgvsp: ENSP00000382921.1:p.Ala262Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3407C>T
  hgvsp: ENSP00000371293.3:p.Ala1136Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1932C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1310C>T
  hgvsp: ENSP00000371285.3:p.Ala437Val
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1067C>T
  hgvsp: ENSP00000297488.6:p.Ala356Val
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18512
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1190Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

8-17504522-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504522
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504522
    reference: chr 8
allele count: 1
allele frequency: 8.289674381590291e-6
allele num: 120632
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1066G>C
  hgvsp: ENSP00000297488.6:p.Ala356Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3406G>C
  hgvsp: ENSP00000371293.3:p.Ala1136Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.784G>C
  hgvsp: ENSP00000382921.1:p.Ala262Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1316G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3568G>C
  hgvsp: ENSP00000262102.6:p.Ala1190Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.266G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3406G>C
  hgvsp: ENSP00000430167.1:p.Ala1136Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.1003G>C
  hgvsp: ENSP00000445738.1:p.Ala335Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.346G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.819G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1309G>C
  hgvsp: ENSP00000371285.3:p.Ala437Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1931G>C
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1190Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum

8-17504531-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504531
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504531
    reference: chr 8
allele count: 1
allele frequency: 8.288575028181154e-6
allele num: 120648
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1057G>C
  hgvsp: ENSP00000297488.6:p.Glu353Gln
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.257G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3397G>C
  hgvsp: ENSP00000371293.3:p.Glu1133Gln
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3397G>C
  hgvsp: ENSP00000430167.1:p.Glu1133Gln
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.810G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1922G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3559G>C
  hgvsp: ENSP00000262102.6:p.Glu1187Gln
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.775G>C
  hgvsp: ENSP00000382921.1:p.Glu259Gln
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1307G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.994G>C
  hgvsp: ENSP00000445738.1:p.Glu332Gln
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1300G>C
  hgvsp: ENSP00000371285.3:p.Glu434Gln
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.337G>C
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1187Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

8-17504542-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504542
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504542
    reference: chr 8
allele count: 2
allele frequency: 1.657687525901368e-5
allele num: 120650
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.983A>G
  hgvsp: ENSP00000445738.1:p.Gln328Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3548A>G
  hgvsp: ENSP00000262102.6:p.Gln1183Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3386A>G
  hgvsp: ENSP00000430167.1:p.Gln1129Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.764A>G
  hgvsp: ENSP00000382921.1:p.Gln255Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.799A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.326A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1296A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1046A>G
  hgvsp: ENSP00000297488.6:p.Gln349Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1911A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1289A>G
  hgvsp: ENSP00000371285.3:p.Gln430Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3386A>G
  hgvsp: ENSP00000371293.3:p.Gln1129Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.246A>G
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln1183Arg
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

8-17504549-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504549
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504549
    reference: chr 8
allele count: 3
allele frequency: 2.486490070616318e-5
allele num: 120652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3379T>C
  hgvsp: ENSP00000371293.3:p.Phe1127Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3541T>C
  hgvsp: ENSP00000262102.6:p.Phe1181Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1904T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.792T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.319T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.757T>C
  hgvsp: ENSP00000382921.1:p.Phe253Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.239T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1039T>C
  hgvsp: ENSP00000297488.6:p.Phe347Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3379T>C
  hgvsp: ENSP00000430167.1:p.Phe1127Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.976T>C
  hgvsp: ENSP00000445738.1:p.Phe326Leu
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1289T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1282T>C
  hgvsp: ENSP00000371285.3:p.Phe428Leu
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe1181Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

8-17504551-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504551
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504551
    reference: chr 8
allele count: 4
allele frequency: 3.315100281783524e-5
allele num: 120660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1287G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3377G>A
  hgvsp: ENSP00000430167.1:p.Arg1126His
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.790G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.237G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.317G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1037G>A
  hgvsp: ENSP00000297488.6:p.Arg346His
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3539G>A
  hgvsp: ENSP00000262102.6:p.Arg1180His
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.974G>A
  hgvsp: ENSP00000445738.1:p.Arg325His
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3377G>A
  hgvsp: ENSP00000371293.3:p.Arg1126His
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.755G>A
  hgvsp: ENSP00000382921.1:p.Arg252His
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1280G>A
  hgvsp: ENSP00000371285.3:p.Arg427His
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1902G>A
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1180His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

8-17504553-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504553
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504553
    reference: chr 8
allele count: 1
allele frequency: 8.287888080359362e-6
allele num: 120658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.315G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1285G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1278G>A
  hgvsp: ENST00000381861.3:c.1278G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3375G>A
  hgvsp: ENST00000381869.3:c.3375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1900G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.753G>A
  hgvsp: ENST00000400046.1:c.753G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1035G>A
  hgvsp: ENST00000297488.6:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.235G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3375G>A
  hgvsp: ENST00000519263.1:c.3375G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.972G>A
  hgvsp: ENST00000544260.1:c.972G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3537G>A
  hgvsp: ENST00000262102.6:c.3537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.788G>A
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys1179Lys
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-17504556-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504556
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504556
    reference: chr 8
allele count: 2
allele frequency: 1.657577616071872e-5
allele num: 120658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.750G>T
  hgvsp: ENSP00000382921.1:p.Leu250Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1032G>T
  hgvsp: ENSP00000297488.6:p.Leu344Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.785G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1897G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.969G>T
  hgvsp: ENSP00000445738.1:p.Leu323Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1275G>T
  hgvsp: ENSP00000371285.3:p.Leu425Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.232G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3372G>T
  hgvsp: ENSP00000371293.3:p.Leu1124Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3372G>T
  hgvsp: ENSP00000430167.1:p.Leu1124Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.312G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3534G>T
  hgvsp: ENSP00000262102.6:p.Leu1178Phe
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1282G>T
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1178Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

8-17504558-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504558
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504558
    reference: chr 8
allele count: 2
allele frequency: 1.657550140891762e-5
allele num: 120660
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3370T>C
  hgvsp: ENST00000519263.1:c.3370T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.230T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.783T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.310T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1030T>C
  hgvsp: ENST00000297488.6:c.1030T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1280T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1895T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.748T>C
  hgvsp: ENST00000400046.1:c.748T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3370T>C
  hgvsp: ENST00000381869.3:c.3370T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1273T>C
  hgvsp: ENST00000381861.3:c.1273T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3532T>C
  hgvsp: ENST00000262102.6:c.3532T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.967T>C
  hgvsp: ENST00000544260.1:c.967T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu1178Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD

8-17504560-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504560
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504560
    reference: chr 8
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.308A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1278A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.746A>G
  hgvsp: ENSP00000382921.1:p.Lys249Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.228A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1028A>G
  hgvsp: ENSP00000297488.6:p.Lys343Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.965A>G
  hgvsp: ENSP00000445738.1:p.Lys322Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3368A>G
  hgvsp: ENSP00000371293.3:p.Lys1123Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3368A>G
  hgvsp: ENSP00000430167.1:p.Lys1123Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1271A>G
  hgvsp: ENSP00000371285.3:p.Lys424Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.781A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3530A>G
  hgvsp: ENSP00000262102.6:p.Lys1177Arg
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1893A>G
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys1177Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/8-17504569-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504569
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504569
    reference: chr 8
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1019T>G
  hgvsp: ENSP00000297488.6:p.Leu340Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.219T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.299T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3359T>G
  hgvsp: ENSP00000430167.1:p.Leu1120Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1262T>G
  hgvsp: ENSP00000371285.3:p.Leu421Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.737T>G
  hgvsp: ENSP00000382921.1:p.Leu246Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.772T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1884T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3521T>G
  hgvsp: ENSP00000262102.6:p.Leu1174Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3359T>G
  hgvsp: ENSP00000371293.3:p.Leu1120Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.956T>G
  hgvsp: ENSP00000445738.1:p.Leu319Trp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1269T>G
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11638
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1174Trp
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

8-17504573-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504573
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504573
    reference: chr 8
allele count: 1
allele frequency: 8.288712431410904e-6
allele num: 120646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1880G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3355G>C
  hgvsp: ENSP00000430167.1:p.Ala1119Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3517G>C
  hgvsp: ENSP00000262102.6:p.Ala1173Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.733G>C
  hgvsp: ENSP00000382921.1:p.Ala245Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.295G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1258G>C
  hgvsp: ENSP00000371285.3:p.Ala420Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3355G>C
  hgvsp: ENSP00000371293.3:p.Ala1119Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1265G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.215G>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1015G>C
  hgvsp: ENSP00000297488.6:p.Ala339Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.952G>C
  hgvsp: ENSP00000445738.1:p.Ala318Pro
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.768G>C
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1173Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

8-17504580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504580
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504580
    reference: chr 8
allele count: 1
allele frequency: 8.290361625574107e-6
allele num: 120622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.726C>T
  hgvsp: ENST00000400046.1:c.726C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1251C>T
  hgvsp: ENST00000381861.3:c.1251C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1258C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3510C>T
  hgvsp: ENST00000262102.6:c.3510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3348C>T
  hgvsp: ENST00000381869.3:c.3348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.761C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.208C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1873C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1008C>T
  hgvsp: ENST00000297488.6:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3348C>T
  hgvsp: ENST00000519263.1:c.3348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.288C>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.945C>T
  hgvsp: ENST00000544260.1:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn1170Asn
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

8-17504582-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504582
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504582
    reference: chr 8
allele count: 1
allele frequency: 8.291186468783682e-6
allele num: 120610
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1871A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.206A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1249A>G
  hgvsp: ENSP00000371285.3:p.Asn417Asp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.286A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.759A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.943A>G
  hgvsp: ENSP00000445738.1:p.Asn315Asp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3346A>G
  hgvsp: ENSP00000371293.3:p.Asn1116Asp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3346A>G
  hgvsp: ENSP00000430167.1:p.Asn1116Asp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.724A>G
  hgvsp: ENSP00000382921.1:p.Asn242Asp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1006A>G
  hgvsp: ENSP00000297488.6:p.Asn336Asp
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1256A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3508A>G
  hgvsp: ENSP00000262102.6:p.Asn1170Asp
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11638
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn1170Asp
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-17504584-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504584
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504584
    reference: chr 8
allele count: 1
allele frequency: 8.291598951941893e-6
allele num: 120604
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3506A>G
  hgvsp: ENSP00000262102.6:p.Asp1169Gly
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3344A>G
  hgvsp: ENSP00000430167.1:p.Asp1115Gly
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1254A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1247A>G
  hgvsp: ENSP00000371285.3:p.Asp416Gly
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.722A>G
  hgvsp: ENSP00000382921.1:p.Asp241Gly
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.204A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3344A>G
  hgvsp: ENSP00000371293.3:p.Asp1115Gly
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1869A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.941A>G
  hgvsp: ENSP00000445738.1:p.Asp314Gly
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.757A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1004A>G
  hgvsp: ENSP00000297488.6:p.Asp335Gly
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.284A>G
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp1169Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/8-17504586-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504586
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504586
    reference: chr 8
allele count: 2
allele frequency: 1.658512314453935e-5
allele num: 120590
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.720G>T
  hgvsp: ENST00000400046.1:c.720G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.202G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3342G>T
  hgvsp: ENST00000381869.3:c.3342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1252G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1002G>T
  hgvsp: ENST00000297488.6:c.1002G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1867G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3504G>T
  hgvsp: ENST00000262102.6:c.3504G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.282G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3342G>T
  hgvsp: ENST00000519263.1:c.3342G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.939G>T
  hgvsp: ENST00000544260.1:c.939G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.755G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1245G>T
  hgvsp: ENST00000381861.3:c.1245G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3504G>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

8-17504592-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504592
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504592
    reference: chr 8
allele count: 21
allele frequency: 1.742333731581043e-4
allele num: 120528
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.196C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-4C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-4C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-4C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-4C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-4C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-4C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-4C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-4C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-4C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-4C>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-4C>A
  variant of: http://identifiers.org/hgnc/29789
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: c.3502-4C>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-17504597-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504597
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504597
    reference: chr 8
allele count: 2
allele frequency: 1.660109235187675e-5
allele num: 120474
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-9T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-9T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-9T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.191T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-9T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-9T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-9T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-9T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-9T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-9T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-9T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-9T>C
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

8-17504600-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504600
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504600
    reference: chr 8
allele count: 13
allele frequency: 1.079823905640003e-4
allele num: 120390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-12G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-12G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-12G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.188G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-12G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-12G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-12G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-12G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-12G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-12G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-12G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-12G>A
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4698
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

8-17504611-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504611
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504611
    reference: chr 8
allele count: 2
allele frequency: 1.666611112962901e-5
allele num: 120004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.177T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-23T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-23T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-23T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-23T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-23T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-23T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-23T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-23T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-23T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-23T>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-23T>C
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16563
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

8-17504612-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504612
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504612
    reference: chr 8
allele count: 1
allele frequency: 8.333611120370679e-6
allele num: 119996
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-24G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.176G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-24G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-24G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-24G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-24G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-24G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-24G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-24G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-24G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-24G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-24G>A
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

8-17504616-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504616
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504616
    reference: chr 8
allele count: 1
allele frequency: 8.36988181726874e-6
allele num: 119476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-28A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.172A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-28A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-28A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-28A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-28A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-28A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-28A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-28A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-28A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-28A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-28A>G
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

8-17504618-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504618
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504618
    reference: chr 8
allele count: 3
allele frequency: 2.511132688251247e-5
allele num: 119468
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-30A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-30A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-30A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-30A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-30A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-30A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-30A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.170A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-30A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-30A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-30A>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-30A>G
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15658
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4605
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/8-17504619-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504619
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504619
    reference: chr 8
allele count: 1
allele frequency: 8.387854386847844e-6
allele num: 119220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-31T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-31T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-31T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.169T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-31T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-31T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-31T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-31T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-31T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-31T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-31T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-31T>G
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

8-17504623-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504623
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504623
    reference: chr 8
allele count: 1
allele frequency: 8.417650128790047e-6
allele num: 118798
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-35A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-35A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-35A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-35A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-35A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-35A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-35A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-35A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-35A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.165A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-35A>C
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-35A>C
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

8-17504626-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504626
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504627
    reference: chr 8
allele count: 400
allele frequency: 4.306354025364425e-3
allele num: 92886
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.161dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-39dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-39dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-39dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-39dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-39dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-39dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-39dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-39dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-39dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-39dupT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-39dupT
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8525
  bin: 2.25e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 1.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 12737
  bin: 2.75e1
  variant carriers: 184
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 3.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

8-17504626-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504626
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504625
    reference: chr 8
allele count: 1796
allele frequency: 1.933552957388627e-2
allele num: 92886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-39delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.161delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-39delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-39delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-39delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-39delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-39delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-39delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-39delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-39delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-39delT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-39delT
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 1.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 8525
  bin: 2.25e1
  variant carriers: 513
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 5.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 1.75e1
  variant carriers: 234
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 3.75e1
  variant carriers: 304
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 4.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 12737
  bin: 2.75e1
  variant carriers: 683
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 5.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 9.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 10580
  bin: 3.25e1
  variant carriers: 448
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: TA
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

8-17504626-TAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504626
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504624
    reference: chr 8
allele count: 2
allele frequency: 2.153177012682213e-5
allele num: 92886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-40_1865-39delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-40_*1250-39delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-40_753-39delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-40_718-39delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-40_280-39delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-40_3340-39delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-40_3340-39delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-40_1243-39delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-40_937-39delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-40_3502-39delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.160_161delTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-40_1000-39delTT
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: TAA
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

8-17504626-TAAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504626
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504622
    reference: chr 8
allele count: 1
allele frequency: 1.076588506341106e-5
allele num: 92886
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3736
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3923
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6969
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10634
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3775
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3818
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2268
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 11310
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 6748
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 51524
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5748
  num of homozygotes: 0
population: Other
population: African
population: Latino
reference allele: TAAAA
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

8-17504627-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504627
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504627
    reference: chr 8
allele count: 27
allele frequency: 3.22157260470111e-4
allele num: 83810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-39T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-39T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-39T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-39T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-39T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.161T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-39T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-39T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-39T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-39T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-39T>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-39T>A
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9643
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11680
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/8-17504633-AAAAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504633
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504629
    reference: chr 8
allele count: 1
allele frequency: 8.486803021301875e-6
allele num: 117830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-49_3340-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-49_280-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-49_3340-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.151_154delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-49_1865-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-49_1000-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-49_753-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-49_*1250-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-49_718-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-49_1243-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-49_3502-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-49_937-46delGTTT
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6653
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: AAAAC
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-17504636-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504636
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504636
    reference: chr 8
allele count: 74
allele frequency: 6.358917952772145e-4
allele num: 116372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-48T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-48T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.152T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-48T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-48T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-48T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-48T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-48T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-48T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-48T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-48T>G
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-48T>G
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10236
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11196
  bin: 2.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 6639
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 12432
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/8-17504637-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504637
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504637
    reference: chr 8
allele count: 87
allele frequency: 7.507766655160511e-4
allele num: 115880
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-49G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-49G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-49G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-49G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-49G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-49G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-49G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.151G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-49G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-49G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-49G>T
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-49G>T
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 12562
  bin: 2.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 11248
  bin: 2.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10049
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-17504637-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 17504637
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 17504637
    reference: chr 8
allele count: 1
allele frequency: 8.629616845012081e-6
allele num: 115880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518889
  gene symbol: MTUS1
  hgvsc: ENST00000518889.1:n.151G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000382921
  ensembl transcript: ENST00000400046
  gene symbol: MTUS1
  hgvsc: ENST00000400046.1:c.718-49G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000430167
  ensembl transcript: ENST00000519263
  gene symbol: MTUS1
  hgvsc: ENST00000519263.1:c.3340-49G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371293
  ensembl transcript: ENST00000381869
  gene symbol: MTUS1
  hgvsc: ENST00000381869.3:c.3340-49G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000297488
  ensembl transcript: ENST00000297488
  gene symbol: MTUS1
  hgvsc: ENST00000297488.6:c.1000-49G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000371285
  ensembl transcript: ENST00000381861
  gene symbol: MTUS1
  hgvsc: ENST00000381861.3:c.1243-49G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000262102
  ensembl transcript: ENST00000262102
  gene symbol: MTUS1
  hgvsc: ENST00000262102.6:c.3502-49G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000518792
  gene symbol: MTUS1
  hgvsc: ENST00000518792.1:n.280-49G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000523471
  gene symbol: MTUS1
  hgvsc: ENST00000523471.1:n.753-49G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000431016
  ensembl transcript: ENST00000520196
  gene symbol: MTUS1
  hgvsc: ENST00000520196.1:c.*1250-49G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl transcript: ENST00000517413
  gene symbol: MTUS1
  hgvsc: ENST00000517413.1:n.1865-49G>A
  variant of: http://identifiers.org/hgnc/29789
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000129422
  ensembl protein: ENSP00000445738
  ensembl transcript: ENST00000544260
  gene symbol: MTUS1
  hgvsc: ENST00000544260.1:c.937-49G>A
  variant of: http://identifiers.org/hgnc/29789
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12562
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 60
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9873
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7787
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2397
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5549
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 75
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16831
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 403
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10182
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 471
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4592
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.232062055591467e-4
allele num: 3094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.761032377001959e-5
allele num: 17358
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0121e1

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.569e0

DP
type: SiteQuality
SIO_000300: 6.94056e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.72e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 2.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.38e-1

GenotypeQuality
all individuals: 2302
bin: 1.75e1
variant carriers: 116

GenotypeQuality
all individuals: 746
bin: 3.25e1
variant carriers: 163

GenotypeQuality
all individuals: 3137
bin: 1.25e1
variant carriers: 110

GenotypeQuality
all individuals: 418
bin: 6.25e1
variant carriers: 167

GenotypeQuality
all individuals: 748
bin: 5.25e1
variant carriers: 418

GenotypeQuality
all individuals: 8940
bin: 7.5e0
variant carriers: 104

GenotypeQuality
all individuals: 905
bin: 2.75e1
variant carriers: 155

GenotypeQuality
all individuals: 32692
bin: 2.5e0
variant carriers: 65

GenotypeQuality
all individuals: 98
bin: 9.25e1
variant carriers: 64

GenotypeQuality
all individuals: 250
bin: 7.25e1
variant carriers: 139

GenotypeQuality
all individuals: 307
bin: 6.75e1
variant carriers: 192

GenotypeQuality
all individuals: 247
bin: 7.75e1
variant carriers: 109

GenotypeQuality
all individuals: 3734
bin: 2.25e1
variant carriers: 140

GenotypeQuality
all individuals: 688
bin: 4.75e1
variant carriers: 344

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 68

GenotypeQuality
all individuals: 363
bin: 9.75e1
variant carriers: 178

GenotypeQuality
all individuals: 119
bin: 8.25e1
variant carriers: 52

GenotypeQuality
all individuals: 739
bin: 3.75e1
variant carriers: 329

GenotypeQuality
all individuals: 737
bin: 4.25e1
variant carriers: 369

Latino
type: Population
allele count: 161
allele frequency: 1.366723259762309e-1
allele num: 1178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 729
allele frequency: 9.384654994850669e-2
allele num: 7768
num of homozygotes: 0

Other
type: Population
allele count: 16
allele frequency: 1.290322580645161e-1
allele num: 124
num of homozygotes: 0

East Asian
type: Population
allele count: 107
allele frequency: 8.057228915662651e-2
allele num: 1328
num of homozygotes: 0

South Asian
type: Population
allele count: 608
allele frequency: 2.426177174780527e-1
allele num: 2506
num of homozygotes: 0

African
type: Population
allele count: 149
allele frequency: 1.059743954480797e-1
allele num: 1406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 34
allele frequency: 2.88135593220339e-2
allele num: 1180
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.406e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

QD
type: SiteQuality
SIO_000300: 2.97e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.28292e5

GenotypeQuality
all individuals: 250
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 8940
bin: 7.5e0
variant carriers: 10

GenotypeQuality
all individuals: 905
bin: 2.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3734
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2302
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 98
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 737
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 748
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 418
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 688
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 119
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 363
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 247
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 746
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3137
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 32692
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 652
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 307
bin: 6.75e1
variant carriers: 7

GenotypeQuality
all individuals: 739
bin: 3.75e1
variant carriers: 1

South Asian
type: Population
allele count: 11
allele frequency: 4.389465283320032e-3
allele num: 2506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1178
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 8.064516129032258e-3
allele num: 124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1328
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.422475106685633e-3
allele num: 1406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.287332646755922e-3
allele num: 7768
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.28292e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.406e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 2.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

GenotypeQuality
all individuals: 688
bin: 4.75e1
variant carriers: 284

GenotypeQuality
all individuals: 2302
bin: 1.75e1
variant carriers: 78

GenotypeQuality
all individuals: 739
bin: 3.75e1
variant carriers: 203

GenotypeQuality
all individuals: 112
bin: 8.75e1
variant carriers: 41

GenotypeQuality
all individuals: 363
bin: 9.75e1
variant carriers: 174

GenotypeQuality
all individuals: 32692
bin: 2.5e0
variant carriers: 68

GenotypeQuality
all individuals: 307
bin: 6.75e1
variant carriers: 89

GenotypeQuality
all individuals: 8940
bin: 7.5e0
variant carriers: 74

GenotypeQuality
all individuals: 905
bin: 2.75e1
variant carriers: 108

GenotypeQuality
all individuals: 3734
bin: 2.25e1
variant carriers: 92

GenotypeQuality
all individuals: 250
bin: 7.25e1
variant carriers: 94

GenotypeQuality
all individuals: 3137
bin: 1.25e1
variant carriers: 92

GenotypeQuality
all individuals: 119
bin: 8.25e1
variant carriers: 57

GenotypeQuality
all individuals: 748
bin: 5.25e1
variant carriers: 292

GenotypeQuality
all individuals: 418
bin: 6.25e1
variant carriers: 171

GenotypeQuality
all individuals: 247
bin: 7.75e1
variant carriers: 122

GenotypeQuality
all individuals: 98
bin: 9.25e1
variant carriers: 31

GenotypeQuality
all individuals: 737
bin: 4.25e1
variant carriers: 283

GenotypeQuality
all individuals: 746
bin: 3.25e1
variant carriers: 156

East Asian
type: Population
allele count: 174
allele frequency: 1.310240963855422e-1
allele num: 1328
num of homozygotes: 0

African
type: Population
allele count: 133
allele frequency: 9.45945945945946e-2
allele num: 1406
num of homozygotes: 0

Latino
type: Population
allele count: 127
allele frequency: 1.078098471986418e-1
allele num: 1178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 981
allele frequency: 1.262873326467559e-1
allele num: 7768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 64
allele frequency: 5.423728813559322e-2
allele num: 1180
num of homozygotes: 0

South Asian
type: Population
allele count: 335
allele frequency: 1.336791699920191e-1
allele num: 2506
num of homozygotes: 0

Other
type: Population
allele count: 17
allele frequency: 1.370967741935484e-1
allele num: 124
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

DP
type: SiteQuality
SIO_000300: 6.28292e5

QD
type: SiteQuality
SIO_000300: 2.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.406e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Latino
type: Population
allele count: 3
allele frequency: 2.546689303904924e-3
allele num: 1178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.317198764160659e-3
allele num: 7768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1180
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.406e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

QD
type: SiteQuality
SIO_000300: 2.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

DP
type: SiteQuality
SIO_000300: 6.28292e5

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7768
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.406e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.28292e5

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.97e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 161
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4208
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2910
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12976
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24355
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4121
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5140
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4040
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.123031252576895e-5
allele num: 24254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8350
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.38e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.74424e5

VQSLOD
type: SiteQuality
SIO_000300: -2.514e0

QD
type: SiteQuality
SIO_000300: 2.584e1

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 13131
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 162
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3165
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 23556
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 783
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4203
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4720
bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 2

GenotypeQuality
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bin: 5.75e1
variant carriers: 3

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 4

GenotypeQuality
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bin: 6.75e1
variant carriers: 3

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5054
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.183050280264369e-5
allele num: 23906
num of homozygotes: 0

South Asian
type: Population
allele count: 50
allele frequency: 6.045949214026602e-3
allele num: 8270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3978
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.54e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 1.329e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

DP
type: SiteQuality
SIO_000300: 5.70718e5

GenotypeQuality
all individuals: 17795
bin: 2.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21780
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 1.262626262626263e-3
allele num: 3960
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3312
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

InbreedingCoeff
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SIO_000300: -2.93e-2

FS
type: SiteQuality
SIO_000300: 7.061e0

QD
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BaseQRankSum
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SIO_000300: 2.64e0

VQSLOD
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SIO_000300: -1.351e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.33e-1

DP
type: SiteQuality
SIO_000300: 5.65424e5

MQ
type: SiteQuality
SIO_000300: 5.878e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3086
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.058680696074464e-5
allele num: 19768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.65359e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.45e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 5.227e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
type: SiteQuality
SIO_000300: 2.324e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4154
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.227e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
type: SiteQuality
SIO_000300: 2.324e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.45e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

DP
type: SiteQuality
SIO_000300: 5.65359e5

GenotypeQuality
all individuals: 117
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12154
bin: 7.5e0
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 69

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 4

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 104
bin: 7.25e1
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GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 9

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18750
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 1.021972406745018e-3
allele num: 3914
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

African
type: Population
allele count: 51
allele frequency: 1.623169955442393e-2
allele num: 3142
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2966
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.11e0

MQ
type: SiteQuality
SIO_000300: 5.988e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.529e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.88e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

DP
type: SiteQuality
SIO_000300: 5.64617e5

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16138
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.037129226301597e-4
allele num: 9642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65332
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-2

DP
type: SiteQuality
SIO_000300: 1.799631e6

MQRankSum
type: SiteQuality
SIO_000300: -5.72e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16138
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65332
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

BaseQRankSum
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SIO_000300: 4.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-2

DP
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SIO_000300: 1.799631e6

QD
type: SiteQuality
SIO_000300: 1.369e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 88
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GenotypeQuality
all individuals: 1417
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 34
allele frequency: 3.521856225398798e-3
allele num: 9654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16250
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.748906386701662e-5
allele num: 11430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.924e0

VQSLOD
type: SiteQuality
SIO_000300: 5.64e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.828824e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.511e1

GenotypeQuality
all individuals: 1503
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8491
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2651
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6112
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 153
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1240
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3978
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1429
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23191
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3282
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9660
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16294
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175640724194686e-4
allele num: 8506
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.2e-2

QD
type: SiteQuality
SIO_000300: 1.141e1

FS
type: SiteQuality
SIO_000300: 3.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.179e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.62e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

DP
type: SiteQuality
SIO_000300: 1.83687e6

GenotypeQuality
all individuals: 2549
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1064
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 162
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23036
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 882
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 155
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 94
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1147
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1413
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1044
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1405
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 941
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3806
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1169
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8255
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3192
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1389
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 6910
bin: 9.75e1
variant carriers: 988

South Asian
type: Population
allele count: 57
allele frequency: 3.517215845982969e-3
allele num: 16206
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.504468196951113e-4
allele num: 11414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.680491551459293e-4
allele num: 6510
num of homozygotes: 0

Other
type: Population
allele count: 9
allele frequency: 1.013513513513514e-2
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.075119319360863e-4
allele num: 9638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 3.971891231286282e-4
allele num: 65460
num of homozygotes: 0

East Asian
type: Population
allele count: 980
allele frequency: 1.155933003066761e-1
allele num: 8478
num of homozygotes: 58

FS
type: SiteQuality
SIO_000300: 9.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.39e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.385e0

DP
type: SiteQuality
SIO_000300: 1.858538e6

QD
type: SiteQuality
SIO_000300: 1.341e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

GenotypeQuality
all individuals: 154
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6008
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1203
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8856
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1209
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3975
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1327
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3356
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.126126126126126e-3
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.051106025934401e-5
allele num: 65550
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.623294858342078e-4
allele num: 11436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.068614213821039e-4
allele num: 16294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

QD
type: SiteQuality
SIO_000300: 1.36e1

FS
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.26e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

DP
type: SiteQuality
SIO_000300: 1.867897e6

GenotypeQuality
all individuals: 26626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6010
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2728
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9127
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4097
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52031135976648e-5
allele num: 65776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.636e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.47e-1

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.48e-1

DP
type: SiteQuality
SIO_000300: 1.878958e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

GenotypeQuality
all individuals: 316
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3430
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27629
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4054
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6013
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1222
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520265134239411e-5
allele num: 65778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.269e0

VQSLOD
type: SiteQuality
SIO_000300: 7.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.351e0

QD
type: SiteQuality
SIO_000300: 1.487e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e-1

DP
type: SiteQuality
SIO_000300: 1.891972e6

GenotypeQuality
all individuals: 3452
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2732
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6017
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4089
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.068680182043856e-4
allele num: 9668
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65842
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.487e0

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

MQRankSum
type: SiteQuality
SIO_000300: -2.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.33e-1

QD
type: SiteQuality
SIO_000300: 1.588e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

DP
type: SiteQuality
SIO_000300: 1.903431e6

GenotypeQuality
all individuals: 99
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2711
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6011
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 337
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3464
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4089
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28624
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9317
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.033912324234905e-4
allele num: 9672
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.591400461557148e-5
allele num: 65864
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

QD
type: SiteQuality
SIO_000300: 3.312e1

MQRankSum
type: SiteQuality
SIO_000300: -3.28e-1

DP
type: SiteQuality
SIO_000300: 1.911558e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.978e-1

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6023
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30190
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4143
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2744
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.431019812811474e-4
allele num: 16454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

FS
type: SiteQuality
SIO_000300: 1.954e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.752e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.925318e6

QD
type: SiteQuality
SIO_000300: 1.271e1

GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6023
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 159
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2744
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4143
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3511
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30190
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 8.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511441613010489e-5
allele num: 66162
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

DP
type: SiteQuality
SIO_000300: 1.925318e6

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.09e-1

FS
type: SiteQuality
SIO_000300: 1.954e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.271e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.752e0

VQSLOD
type: SiteQuality
SIO_000300: 3.56e0

GenotypeQuality
all individuals: 2755
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6022
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3521
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9685
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30572
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4157
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.018047926601074e-5
allele num: 66268
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

QD
type: SiteQuality
SIO_000300: 1.259e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 3.157e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

DP
type: SiteQuality
SIO_000300: 1.929055e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e-1

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4158
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9745
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6017
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3536
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30900
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2744
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506977304921788e-5
allele num: 66358
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.702e0

DP
type: SiteQuality
SIO_000300: 1.934216e6

MQ
type: SiteQuality
SIO_000300: 5.503e1

MQRankSum
type: SiteQuality
SIO_000300: 2.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

FS
type: SiteQuality
SIO_000300: 9.419999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.84e-1

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

GenotypeQuality
all individuals: 1242
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3533
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4158
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6018
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9753
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212121212121212e-4
allele num: 16500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

FS
type: SiteQuality
SIO_000300: 5.449e0

QD
type: SiteQuality
SIO_000300: 1.544e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.748e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: 4.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

DP
type: SiteQuality
SIO_000300: 1.934753e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6017
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9766
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3534
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2744
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4161
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30986
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.025851456709069e-4
allele num: 9748
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.327e0

DP
type: SiteQuality
SIO_000300: 1.935397e6

VQSLOD
type: SiteQuality
SIO_000300: 2.01e-1

FS
type: SiteQuality
SIO_000300: 6.35e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.358e0

QD
type: SiteQuality
SIO_000300: 1.005e1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31021
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4164
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2748
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6020
bin: 9.75e1
variant carriers: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.423654871546292e-4
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

DP
type: SiteQuality
SIO_000300: 1.935744e6

QD
type: SiteQuality
SIO_000300: 1.403e1

MQ
type: SiteQuality
SIO_000300: 5.929e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 8.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

FS
type: SiteQuality
SIO_000300: 1.907e0

GenotypeDepth
all individuals: 1165
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 825
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18439
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2746
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3534
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9785
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31151
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4159
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6019
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.945e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

ReadPosRankSum
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SIO_000300: 9.06e-1

MQRankSum
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SIO_000300: 6.73e-1

DP
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SIO_000300: 1.937821e6

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.503e0

QD
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SIO_000300: 1.853e1

FS
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SIO_000300: 3.808e0

ClippingRankSum
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SIO_000300: -3.91e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.003995313767311e-5
allele num: 66578
num of homozygotes: 0

Other
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South Asian
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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VQSLOD
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QD
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FS
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SIO_000300: 8.03e-1

MQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 5.974e1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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MQRankSum
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SIO_000300: 3.42e-1

DP
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SIO_000300: 1.938866e6

QD
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FS
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SIO_000300: 8.03e-1

BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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SIO_000300: 5.974e1

VQSLOD
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SIO_000300: 5.79e-1

ReadPosRankSum
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SIO_000300: 1.56e0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

South Asian
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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Other
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FS
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SIO_000300: 1.264e0

InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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DP
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QD
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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num of homozygotes: 0

Latino
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South Asian
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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FS
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

Other
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African
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Latino
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European (Finnish)
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South Asian
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East Asian
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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BaseQRankSum
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QD
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

African
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European (Non-Finnish)
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Latino
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Other
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East Asian
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South Asian
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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QD
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MQ
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DP
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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Other
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MQRankSum
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ClippingRankSum
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VQSLOD
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SIO_000300: 5.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.424e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

DP
type: SiteQuality
SIO_000300: 1.940626e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 2.448e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

GenotypeDepth
all individuals: 825
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 975
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 469
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4163
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6017
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 82
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2746
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3538
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31307
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9788
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.583e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.75e-1

FS
type: SiteQuality
SIO_000300: 7.371e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

QD
type: SiteQuality
SIO_000300: 1.233e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

MQ
type: SiteQuality
SIO_000300: 5.914e1

DP
type: SiteQuality
SIO_000300: 1.940545e6

GenotypeDepth
all individuals: 469
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2102
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variant carriers: 0

GenotypeDepth
all individuals: 975
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3537
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9791
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31303
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6018
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499910001799964e-5
allele num: 66668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

QD
type: SiteQuality
SIO_000300: 1.267e1

MQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

FS
type: SiteQuality
SIO_000300: 4.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

DP
type: SiteQuality
SIO_000300: 1.940646e6

GenotypeDepth
all individuals: 517
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 162
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variant carriers: 0

GenotypeDepth
all individuals: 4690
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4161
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31302
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6019
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3538
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9792
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.637143519591931e-4
allele num: 8626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

FS
type: SiteQuality
SIO_000300: 2.612e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

DP
type: SiteQuality
SIO_000300: 1.94075e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.19e-1

QD
type: SiteQuality
SIO_000300: 8.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

GenotypeDepth
all individuals: 4690
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 183
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 973
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6015
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variant carriers: 1

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1451
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variant carriers: 0

GenotypeQuality
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 31303
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4160
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3536
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
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: 11562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.495e0

FS
type: SiteQuality
SIO_000300: 6.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

DP
type: SiteQuality
SIO_000300: 1.940571e6

VQSLOD
type: SiteQuality
SIO_000300: -2.135e0

MQRankSum
type: SiteQuality
SIO_000300: -1.886e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.08e0

QD
type: SiteQuality
SIO_000300: 1.417e1

GenotypeDepth
all individuals: 18461
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11641
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1167
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1449
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3536
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31297
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9791
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6017
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1246
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4161
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 3.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.491e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.91e-1

DP
type: SiteQuality
SIO_000300: 1.940575e6

QD
type: SiteQuality
SIO_000300: 1.102e1

GenotypeDepth
all individuals: 1167
bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31310
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999670036296008e-5
allele num: 66674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

DP
type: SiteQuality
SIO_000300: 1.940586e6

VQSLOD
type: SiteQuality
SIO_000300: -7.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

FS
type: SiteQuality
SIO_000300: 8.132999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
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SIO_000300: 1.74e0

QD
type: SiteQuality
SIO_000300: 1.369e1

GenotypeDepth
all individuals: 825
bin: 5.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
all individuals: 4160
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 6016
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021450459652707e-4
allele num: 9790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.285e1

MQRankSum
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SIO_000300: 2.43e0

DP
type: SiteQuality
SIO_000300: 1.940425e6

MQ
type: SiteQuality
SIO_000300: 5.9e1

FS
type: SiteQuality
SIO_000300: 2.789e0

ReadPosRankSum
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SIO_000300: 1.08e0

BaseQRankSum
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SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.183e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.366e0

GenotypeDepth
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bin: 9.25e1
variant carriers: 1

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
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SIO_000300: -8.54e-1

VQSLOD
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BaseQRankSum
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MQ
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SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 1.977e0

InbreedingCoeff
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SIO_000300: 1.53e-2

QD
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DP
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SIO_000300: 1.94011e6

MQRankSum
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SIO_000300: 1.27e-1

ReadPosRankSum
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SIO_000300: 1.11e0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 1.62e-2

ReadPosRankSum
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MQRankSum
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SIO_000300: -8.42e-1

DP
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SIO_000300: 1.939807e6

BaseQRankSum
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SIO_000300: -7.1e-1

ClippingRankSum
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SIO_000300: -7.43e-1

FS
type: SiteQuality
SIO_000300: 1.608e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

GenotypeDepth
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bin: 9.75e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: -7.099999999999999e-2

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -3.439e0

DP
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SIO_000300: 1.939468e6

MQRankSum
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SIO_000300: 6.51e-1

ClippingRankSum
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SIO_000300: -7.05e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.433e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.5184e1

VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.938913e6

QD
type: SiteQuality
SIO_000300: 1.504e1

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

Other
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele frequency: 3.001741009785676e-5
allele num: 66628
num of homozygotes: 0

African
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allele count: 0
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East Asian
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Latino
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num of homozygotes: 0

South Asian
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ClippingRankSum
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DP
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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QD
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.045408058907752e-4
allele num: 9778
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 19
allele frequency: 2.8537098227696e-4
allele num: 66580
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

BaseQRankSum
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SIO_000300: -2.794e0

MQRankSum
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SIO_000300: 1.0e-1

VQSLOD
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QD
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DP
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SIO_000300: 1.937575e6

FS
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SIO_000300: 7.96e-1

ClippingRankSum
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SIO_000300: 4.0e-2

MQ
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SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
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allele frequency: 2.046245140167792e-4
allele num: 9774
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: -1.62e-1

ReadPosRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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FS
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SIO_000300: 1.042e0

DP
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SIO_000300: 1.934896e6

MQRankSum
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SIO_000300: -1.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.305e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.509171116786627e-3
allele num: 8614
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.122e1

VQSLOD
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MQ
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SIO_000300: 5.964e1

ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -3.338e0

FS
type: SiteQuality
SIO_000300: 9.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-2

InbreedingCoeff
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SIO_000300: 4.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 2.329916123019571e-4
allele num: 8584
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66264
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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VQSLOD
type: SiteQuality
SIO_000300: 2.98e-1

MQ
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SIO_000300: 5.967e1

BaseQRankSum
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SIO_000300: 3.27e0

FS
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MQRankSum
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SIO_000300: -4.58e-1

InbreedingCoeff
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ClippingRankSum
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SIO_000300: -3.58e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.905733e6

QD
type: SiteQuality
SIO_000300: 1.702e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509160604871571e-5
allele num: 66262
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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ClippingRankSum
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FS
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DP
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MQRankSum
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QD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 1.032631144155308e-4
allele num: 9684
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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Other
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BaseQRankSum
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ReadPosRankSum
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FS
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DP
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ClippingRankSum
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MQRankSum
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QD
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MQ
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

African
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Latino
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Other
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South Asian
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European (Finnish)
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European (Non-Finnish)
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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QD
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FS
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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South Asian
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European (Non-Finnish)
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African
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InbreedingCoeff
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DP
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SIO_000300: 1.864487e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.31e-1

FS
type: SiteQuality
SIO_000300: 5.266e0

QD
type: SiteQuality
SIO_000300: 1.934e1

MQRankSum
type: SiteQuality
SIO_000300: -3.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.99e0

VQSLOD
type: SiteQuality
SIO_000300: -1.059e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 307
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variant carriers: 0

GenotypeQuality
all individuals: 2277
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 531
bin: 5.75e1
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GenotypeQuality
all individuals: 2703
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.191895113230036e-4
allele num: 8390
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 7.93e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

DP
type: SiteQuality
SIO_000300: 1.8588e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.536e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeDepth
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bin: 3.25e1
variant carriers: 114

GenotypeQuality
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bin: 2.75e1
variant carriers: 72

GenotypeQuality
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bin: 6.25e1
variant carriers: 7

GenotypeQuality
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bin: 1.75e1
variant carriers: 93

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 11

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 27

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3736
bin: 3.25e1
variant carriers: 62

GenotypeQuality
all individuals: 3923
bin: 9.75e1
variant carriers: 21

Other
type: Population
allele count: 3
allele frequency: 4.178272980501393e-3
allele num: 718
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 2.158600318109521e-3
allele num: 8802
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.617720258835241e-3
allele num: 8036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.479471120389701e-4
allele num: 5748
num of homozygotes: 0

South Asian
type: Population
allele count: 203
allele frequency: 1.794871794871795e-2
allele num: 11310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 154
allele frequency: 2.988898377455166e-3
allele num: 51524
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 8.891523414344991e-4
allele num: 6748
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.975966e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.72e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

GenotypeDepth
all individuals: 338
bin: 7.75e1
variant carriers: 19

GenotypeQuality
all individuals: 3736
bin: 3.25e1
variant carriers: 233

GenotypeQuality
all individuals: 1546
bin: 5.25e1
variant carriers: 100

GenotypeQuality
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bin: 9.75e1
variant carriers: 211

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 2900
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GenotypeQuality
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variant carriers: 36

GenotypeQuality
all individuals: 3775
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GenotypeQuality
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GenotypeQuality
all individuals: 10634
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GenotypeQuality
all individuals: 2159
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GenotypeQuality
all individuals: 2100
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variant carriers: 120

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 903
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variant carriers: 73

GenotypeQuality
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GenotypeQuality
all individuals: 1585
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variant carriers: 256

GenotypeQuality
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variant carriers: 143

GenotypeQuality
all individuals: 1086
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variant carriers: 23

GenotypeQuality
all individuals: 1696
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variant carriers: 42

GenotypeQuality
all individuals: 626
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variant carriers: 27

GenotypeQuality
all individuals: 3146
bin: 3.75e1
variant carriers: 177

European (Finnish)
type: Population
allele count: 35
allele frequency: 6.089074460681976e-3
allele num: 5748
num of homozygotes: 0

Latino
type: Population
allele count: 168
allele frequency: 1.90865712338105e-2
allele num: 8802
num of homozygotes: 0

African
type: Population
allele count: 100
allele frequency: 1.244400199104032e-2
allele num: 8036
num of homozygotes: 0

South Asian
type: Population
allele count: 243
allele frequency: 2.148541114058355e-2
allele num: 11310
num of homozygotes: 0

East Asian
type: Population
allele count: 101
allele frequency: 1.496739774748074e-2
allele num: 6748
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 1.671309192200557e-2
allele num: 718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1137
allele frequency: 2.20673860725099e-2
allele num: 51524
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

QD
type: SiteQuality
SIO_000300: 7.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.72e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

DP
type: SiteQuality
SIO_000300: 1.975966e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

GenotypeDepth
all individuals: 8525
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3775
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variant carriers: 0

GenotypeQuality
all individuals: 3923
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variant carriers: 0

GenotypeQuality
all individuals: 1086
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1585
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variant carriers: 0

GenotypeQuality
all individuals: 903
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.88168620448723e-5
allele num: 51524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5748
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

ReadPosRankSum
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SIO_000300: -1.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

DP
type: SiteQuality
SIO_000300: 1.975966e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.72e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.136105430583958e-4
allele num: 8802
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.72e-2

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.975966e6

QD
type: SiteQuality
SIO_000300: 7.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 165
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variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
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GenotypeQuality
all individuals: 1725
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2062
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GenotypeQuality
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GenotypeQuality
all individuals: 3599
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variant carriers: 28

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3048
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GenotypeQuality
all individuals: 558
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7372
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.143163309044149e-5
allele num: 46660
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.77453447408153e-4
allele num: 7948
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5550
num of homozygotes: 0

South Asian
type: Population
allele count: 23
allele frequency: 2.444208289054197e-3
allele num: 9410
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.29e-2

DP
type: SiteQuality
SIO_000300: 1.833633e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

QD
type: SiteQuality
SIO_000300: 8.42e0

GenotypeDepth
all individuals: 918
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variant carriers: 0

GenotypeQuality
all individuals: 427
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GenotypeQuality
all individuals: 1774
bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5915
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GenotypeQuality
all individuals: 758
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GenotypeQuality
all individuals: 2674
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542257865515114e-5
allele num: 64840
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.13e0

DP
type: SiteQuality
SIO_000300: 1.865362e6

MQ
type: SiteQuality
SIO_000300: 5.472e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.99e0

MQRankSum
type: SiteQuality
SIO_000300: -2.188e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.453e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.078e0

GenotypeDepth
all individuals: 379
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variant carriers: 1

GenotypeQuality
all individuals: 13075
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3465
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
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variant carriers: 0

GenotypeQuality
all individuals: 2267
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3090
bin: 2.25e1
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GenotypeQuality
all individuals: 3746
bin: 4.75e1
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GenotypeQuality
all individuals: 2614
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GenotypeQuality
all individuals: 3133
bin: 3.25e1
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GenotypeQuality
all individuals: 3043
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GenotypeQuality
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GenotypeQuality
all individuals: 6558
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GenotypeQuality
all individuals: 330
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GenotypeQuality
all individuals: 2138
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GenotypeQuality
all individuals: 5958
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GenotypeQuality
all individuals: 680
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GenotypeQuality
all individuals: 1409
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GenotypeQuality
all individuals: 528
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GenotypeQuality
all individuals: 2575
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GenotypeQuality
all individuals: 1226
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GenotypeQuality
all individuals: 3577
bin: 7.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.704897706137632e-3
allele num: 6452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 61
allele frequency: 9.534527493826003e-4
allele num: 63978
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.057305984351871e-4
allele num: 9458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.143260842855388e-5
allele num: 16278
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

VQSLOD
type: SiteQuality
SIO_000300: 4.15e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.862372e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

QD
type: SiteQuality
SIO_000300: 1.085e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 918
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 754
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3570
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 441
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6032
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2973
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3503
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2579
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 10620
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5946
bin: 9.75e1
variant carriers: 76

GenotypeQuality
all individuals: 4105
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1347
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1403
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4406
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 15
allele frequency: 1.870790720878024e-3
allele num: 8018
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.293577981651376e-3
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.645401052957572e-4
allele num: 6458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 41
allele frequency: 6.433592769269395e-4
allele num: 63728
num of homozygotes: 0

South Asian
type: Population
allele count: 16
allele frequency: 9.903441445902451e-4
allele num: 16156
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.783166904422254e-4
allele num: 11216
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 8.481764206955047e-4
allele num: 9432
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

DP
type: SiteQuality
SIO_000300: 1.85998e6

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.971e0

GenotypeDepth
all individuals: 245
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 1.75e1
variant carriers: 0