8-125568501-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568501
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568501
    reference: chr 8
allele count: 2
allele frequency: 1.66306336271412e-5
allele num: 120260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.461G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.530G>A
  hgvsp: ENSP00000393606.2:p.Arg177Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.698G>A
  hgvsp: ENSP00000378884.2:p.Arg233Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.530G>A
  hgvsp: ENSP00000346119.4:p.Arg177Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.723G>A
  hgvsp: ENSP00000428348.1:p.Arg242Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1301G>A
  hgvsp: ENSP00000367256.3:p.Arg434Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1046G>A
  hgvsp: ENSP00000428319.1:p.Arg349Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.649G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1376G>A
  hgvsp: ENSP00000429064.1:p.Arg459Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1388G>A
  hgvsp: ENSP00000322804.5:p.Arg463Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.313G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.738G>A
  hgvsp: ENSP00000428685.1:p.Arg247Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9147C>T
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg459Gln
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-125568502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568502
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568502
    reference: chr 8
allele count: 64
allele frequency: 5.319856363878176e-4
allele num: 120304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.529C>T
  hgvsp: ENSP00000346119.4:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1045C>T
  hgvsp: ENSP00000428319.1:p.Arg349Trp
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.648C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.312C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.460C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9148G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.529C>T
  hgvsp: ENSP00000393606.2:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.697C>T
  hgvsp: ENSP00000378884.2:p.Arg233Trp
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1375C>T
  hgvsp: ENSP00000429064.1:p.Arg459Trp
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.559C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1387C>T
  hgvsp: ENSP00000322804.5:p.Arg463Trp
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.722C>T
  hgvsp: ENSP00000428348.1:p.Arg242Trp
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.737C>T
  hgvsp: ENSP00000428685.1:p.Arg247Trp
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1300C>T
  hgvsp: ENSP00000367256.3:p.Arg434Trp
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14791
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 40132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg459Trp
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

8-125568503-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568503
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568503
    reference: chr 8
allele count: 4
allele frequency: 3.324026060364313e-5
allele num: 120336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.528A>G
  hgvsp: ENST00000354184.4:c.528A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.558A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.311A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1374A>G
  hgvsp: ENST00000518547.1:c.1374A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1044A>G
  hgvsp: ENST00000524090.1:c.1044A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.528A>G
  hgvsp: ENST00000431961.2:c.528A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.721A>G
  hgvsp: ENST00000523179.1:c.721A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.459A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.696A>G
  hgvsp: ENST00000395508.2:c.696A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1386A>G
  hgvsp: ENST00000325064.5:c.1386A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.736A>G
  hgvsp: ENST00000519168.1:c.736A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9149T>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.647A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1299A>G
  hgvsp: ENST00000378017.3:c.1299A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40156
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro458Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

8-125568506-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568506
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568506
    reference: chr 8
allele count: 1
allele frequency: 8.30827005200977e-6
allele num: 120362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1383A>G
  hgvsp: ENST00000325064.5:c.1383A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9152T>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.308A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.644A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.555A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1041A>G
  hgvsp: ENST00000524090.1:c.1041A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.525A>G
  hgvsp: ENST00000354184.4:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1371A>G
  hgvsp: ENST00000518547.1:c.1371A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.456A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.733A>G
  hgvsp: ENST00000519168.1:c.733A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.525A>G
  hgvsp: ENST00000431961.2:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.693A>G
  hgvsp: ENST00000395508.2:c.693A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.718A>G
  hgvsp: ENST00000523179.1:c.718A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1296A>G
  hgvsp: ENST00000378017.3:c.1296A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg457Arg
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

8-125568511-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568511
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568511
    reference: chr 8
allele count: 2
allele frequency: 1.660770929865644e-5
allele num: 120426
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1366C>G
  hgvsp: ENSP00000429064.1:p.Gln456Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.639C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.451C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.520C>G
  hgvsp: ENSP00000393606.2:p.Gln174Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.713C>G
  hgvsp: ENSP00000428348.1:p.Gln239Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.688C>G
  hgvsp: ENSP00000378884.2:p.Gln230Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1291C>G
  hgvsp: ENSP00000367256.3:p.Gln431Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.728C>G
  hgvsp: ENSP00000428685.1:p.Gln244Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1036C>G
  hgvsp: ENSP00000428319.1:p.Gln346Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.550C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9157G>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1378C>G
  hgvsp: ENSP00000322804.5:p.Gln460Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.520C>G
  hgvsp: ENSP00000346119.4:p.Gln174Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.303C>G
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln456Glu
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: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/8-125568512-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568512
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568512
    reference: chr 8
allele count: 1
allele frequency: 8.303027283747654e-6
allele num: 120438
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.727T>G
  hgvsp: ENST00000519168.1:c.727T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.687T>G
  hgvsp: ENST00000395508.2:c.687T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.519T>G
  hgvsp: ENST00000431961.2:c.519T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.302T>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.638T>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1377T>G
  hgvsp: ENST00000325064.5:c.1377T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.549T>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.519T>G
  hgvsp: ENST00000354184.4:c.519T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9158A>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1290T>G
  hgvsp: ENST00000378017.3:c.1290T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.450T>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1035T>G
  hgvsp: ENST00000524090.1:c.1035T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1365T>G
  hgvsp: ENST00000518547.1:c.1365T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.712T>G
  hgvsp: ENST00000523179.1:c.712T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala455Ala
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

8-125568516-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568516
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568516
    reference: chr 8
allele count: 5
allele frequency: 4.150686523550995e-5
allele num: 120462
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1361A>C
  hgvsp: ENSP00000429064.1:p.Glu454Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.515A>C
  hgvsp: ENSP00000346119.4:p.Glu172Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9162T>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.723A>C
  hgvsp: ENSP00000428685.1:p.Glu242Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.708A>C
  hgvsp: ENSP00000428348.1:p.Glu237Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.298A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.683A>C
  hgvsp: ENSP00000378884.2:p.Glu228Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1031A>C
  hgvsp: ENSP00000428319.1:p.Glu344Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.634A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1286A>C
  hgvsp: ENSP00000367256.3:p.Glu429Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1373A>C
  hgvsp: ENSP00000322804.5:p.Glu458Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.446A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.515A>C
  hgvsp: ENSP00000393606.2:p.Glu172Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.545A>C
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39661
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu454Ala
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

8-125568522-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568522
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568522
    reference: chr 8
allele count: 2
allele frequency: 1.659861235600704e-5
allele num: 120492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.509C>T
  hgvsp: ENSP00000393606.2:p.Ala170Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.509C>T
  hgvsp: ENSP00000346119.4:p.Ala170Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1025C>T
  hgvsp: ENSP00000428319.1:p.Ala342Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.539C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1280C>T
  hgvsp: ENSP00000367256.3:p.Ala427Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1355C>T
  hgvsp: ENSP00000429064.1:p.Ala452Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1367C>T
  hgvsp: ENSP00000322804.5:p.Ala456Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.292C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.702C>T
  hgvsp: ENSP00000428348.1:p.Ala235Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9168G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.677C>T
  hgvsp: ENSP00000378884.2:p.Ala226Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.628C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.717C>T
  hgvsp: ENSP00000428685.1:p.Ala240Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.440C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala452Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS

8-125568538-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568538
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568538
    reference: chr 8
allele count: 1
allele frequency: 8.304130474498016e-6
allele num: 120422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.661G>A
  hgvsp: ENSP00000378884.2:p.Gly221Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.276G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.493G>A
  hgvsp: ENSP00000393606.2:p.Gly165Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1009G>A
  hgvsp: ENSP00000428319.1:p.Gly337Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1264G>A
  hgvsp: ENSP00000367256.3:p.Gly422Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.493G>A
  hgvsp: ENSP00000346119.4:p.Gly165Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.523G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1339G>A
  hgvsp: ENSP00000429064.1:p.Gly447Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9184C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1351G>A
  hgvsp: ENSP00000322804.5:p.Gly451Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.686G>A
  hgvsp: ENSP00000428348.1:p.Gly230Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.701G>A
  hgvsp: ENSP00000428685.1:p.Gly235Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.424G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.612G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly447Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

8-125568539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568539
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568539
    reference: chr 8
allele count: 13
allele frequency: 1.079716283782661e-4
allele num: 120402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1008C>T
  hgvsp: ENST00000524090.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.685C>T
  hgvsp: ENST00000523179.1:c.685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9185G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.492C>T
  hgvsp: ENST00000354184.4:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1263C>T
  hgvsp: ENST00000378017.3:c.1263C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1338C>T
  hgvsp: ENST00000518547.1:c.1338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.660C>T
  hgvsp: ENST00000395508.2:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1350C>T
  hgvsp: ENST00000325064.5:c.1350C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.492C>T
  hgvsp: ENST00000431961.2:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.275C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.423C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.611C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.700C>T
  hgvsp: ENST00000519168.1:c.700C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.522C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15177
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser446Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

8-125568541-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568541
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568541
    reference: chr 8
allele count: 3
allele frequency: 2.491280518186348e-5
allele num: 120420
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.658A>G
  hgvsp: ENSP00000378884.2:p.Ser220Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.609A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.698A>G
  hgvsp: ENSP00000428685.1:p.Ser234Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1261A>G
  hgvsp: ENSP00000367256.3:p.Ser421Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.520A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1348A>G
  hgvsp: ENSP00000322804.5:p.Ser450Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9187T>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.490A>G
  hgvsp: ENSP00000393606.2:p.Ser164Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1336A>G
  hgvsp: ENSP00000429064.1:p.Ser446Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.490A>G
  hgvsp: ENSP00000346119.4:p.Ser164Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.421A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.683A>G
  hgvsp: ENSP00000428348.1:p.Ser229Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1006A>G
  hgvsp: ENSP00000428319.1:p.Ser336Gly
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.273A>G
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38116
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser446Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

8-125568544-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568544
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568544
    reference: chr 8
allele count: 5
allele frequency: 4.15337586390218e-5
allele num: 120384
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1333G>A
  hgvsp: ENSP00000429064.1:p.Ala445Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1258G>A
  hgvsp: ENSP00000367256.3:p.Ala420Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.606G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.270G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.517G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.655G>A
  hgvsp: ENSP00000378884.2:p.Ala219Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1003G>A
  hgvsp: ENSP00000428319.1:p.Ala335Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1345G>A
  hgvsp: ENSP00000322804.5:p.Ala449Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9190C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.680G>A
  hgvsp: ENSP00000428348.1:p.Ala228Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.695G>A
  hgvsp: ENSP00000428685.1:p.Ala233Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.487G>A
  hgvsp: ENSP00000393606.2:p.Ala163Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.487G>A
  hgvsp: ENSP00000346119.4:p.Ala163Thr
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.418G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38094
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15236
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala445Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

8-125568545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568545
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568545
    reference: chr 8
allele count: 6
allele frequency: 4.984547901505333e-5
allele num: 120372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1257C>T
  hgvsp: ENST00000378017.3:c.1257C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.269C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1002C>T
  hgvsp: ENST00000524090.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.654C>T
  hgvsp: ENST00000395508.2:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1332C>T
  hgvsp: ENST00000518547.1:c.1332C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.516C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9191G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.417C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.694C>T
  hgvsp: ENST00000519168.1:c.694C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.486C>T
  hgvsp: ENST00000354184.4:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.679C>T
  hgvsp: ENST00000523179.1:c.679C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.605C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1344C>T
  hgvsp: ENST00000325064.5:c.1344C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.486C>T
  hgvsp: ENST00000431961.2:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr444Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

8-125568546-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568546
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568546
    reference: chr 8
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1343C>A
  hgvsp: ENSP00000322804.5:p.Thr448Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1256C>A
  hgvsp: ENSP00000367256.3:p.Thr419Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.604C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.693C>A
  hgvsp: ENSP00000428685.1:p.Thr232Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.485C>A
  hgvsp: ENSP00000393606.2:p.Thr162Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.1001C>A
  hgvsp: ENSP00000428319.1:p.Thr334Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.268C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.485C>A
  hgvsp: ENSP00000346119.4:p.Thr162Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.416C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.678C>A
  hgvsp: ENSP00000428348.1:p.Thr227Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.653C>A
  hgvsp: ENSP00000378884.2:p.Thr218Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.515C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9192G>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1331C>A
  hgvsp: ENSP00000429064.1:p.Thr444Asn
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr444Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP

8-125568548-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568548
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568548
    reference: chr 8
allele count: 1
allele frequency: 8.304682179812978e-6
allele num: 120414
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.483T>C
  hgvsp: ENST00000354184.4:c.483T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1329T>C
  hgvsp: ENST00000518547.1:c.1329T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.691T>C
  hgvsp: ENST00000519168.1:c.691T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1341T>C
  hgvsp: ENST00000325064.5:c.1341T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.602T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.999T>C
  hgvsp: ENST00000524090.1:c.999T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1254T>C
  hgvsp: ENST00000378017.3:c.1254T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.651T>C
  hgvsp: ENST00000395508.2:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.513T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.414T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.266T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.483T>C
  hgvsp: ENST00000431961.2:c.483T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.676T>C
  hgvsp: ENST00000523179.1:c.676T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9194A>G
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr443Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

8-125568562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568562
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568562
    reference: chr 8
allele count: 5
allele frequency: 4.158488306330882e-5
allele num: 120236
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1315G>A
  hgvsp: ENSP00000429064.1:p.Gly439Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.252G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.677G>A
  hgvsp: ENSP00000428685.1:p.Gly227Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1327G>A
  hgvsp: ENSP00000322804.5:p.Gly443Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1240G>A
  hgvsp: ENSP00000367256.3:p.Gly414Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.985G>A
  hgvsp: ENSP00000428319.1:p.Gly329Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.637G>A
  hgvsp: ENSP00000378884.2:p.Gly213Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.588G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.469G>A
  hgvsp: ENSP00000346119.4:p.Gly157Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.469G>A
  hgvsp: ENSP00000393606.2:p.Gly157Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9208C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.662G>A
  hgvsp: ENSP00000428348.1:p.Gly222Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.400G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.499G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37204
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly439Arg
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

8-125568563-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568563
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568563
    reference: chr 8
allele count: 1
allele frequency: 8.312690152787244e-6
allele num: 120298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.984C>T
  hgvsp: ENST00000524090.1:c.984C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1326C>T
  hgvsp: ENST00000325064.5:c.1326C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.251C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.636C>T
  hgvsp: ENST00000395508.2:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1314C>T
  hgvsp: ENST00000518547.1:c.1314C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.676C>T
  hgvsp: ENST00000519168.1:c.676C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.399C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.498C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1239C>T
  hgvsp: ENST00000378017.3:c.1239C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.661C>T
  hgvsp: ENST00000523179.1:c.661C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.468C>T
  hgvsp: ENST00000354184.4:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.587C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.468C>T
  hgvsp: ENST00000431961.2:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9209G>A
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn438Asn
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: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

8-125568572-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568572
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568572
    reference: chr 8
allele count: 2
allele frequency: 1.662897432486364e-5
allele num: 120272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.975G>A
  hgvsp: ENST00000524090.1:c.975G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.459G>A
  hgvsp: ENST00000354184.4:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1230G>A
  hgvsp: ENST00000378017.3:c.1230G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.667G>A
  hgvsp: ENST00000519168.1:c.667G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.652G>A
  hgvsp: ENST00000523179.1:c.652G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1317G>A
  hgvsp: ENST00000325064.5:c.1317G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.627G>A
  hgvsp: ENST00000395508.2:c.627G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.578G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1305G>A
  hgvsp: ENST00000518547.1:c.1305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.390G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.242G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.459G>A
  hgvsp: ENST00000431961.2:c.459G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9218C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.489G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16021
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro435Pro
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

8-125568573-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568573
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568573
    reference: chr 8
allele count: 52
allele frequency: 4.324683965402528e-4
allele num: 120240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.651C>T
  hgvsp: ENSP00000428348.1:p.Pro218Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.241C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.389C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.626C>T
  hgvsp: ENSP00000378884.2:p.Pro209Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1304C>T
  hgvsp: ENSP00000429064.1:p.Pro435Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1229C>T
  hgvsp: ENSP00000367256.3:p.Pro410Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.666C>T
  hgvsp: ENSP00000428685.1:p.Pro223Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1316C>T
  hgvsp: ENSP00000322804.5:p.Pro439Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.974C>T
  hgvsp: ENSP00000428319.1:p.Pro325Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9219G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.458C>T
  hgvsp: ENSP00000393606.2:p.Pro153Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.458C>T
  hgvsp: ENSP00000346119.4:p.Pro153Leu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.577C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.488C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16043
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37382
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Pro435Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum

8-125568573-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568573
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568573
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 120240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1229C>A
  hgvsp: ENSP00000367256.3:p.Pro410Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1316C>A
  hgvsp: ENSP00000322804.5:p.Pro439Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.651C>A
  hgvsp: ENSP00000428348.1:p.Pro218Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.458C>A
  hgvsp: ENSP00000346119.4:p.Pro153Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.458C>A
  hgvsp: ENSP00000393606.2:p.Pro153Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1304C>A
  hgvsp: ENSP00000429064.1:p.Pro435Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.389C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.577C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.974C>A
  hgvsp: ENSP00000428319.1:p.Pro325Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.626C>A
  hgvsp: ENSP00000378884.2:p.Pro209Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.241C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9219G>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.488C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.666C>A
  hgvsp: ENSP00000428685.1:p.Pro223Gln
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16043
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro435Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-125568574-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568574
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568574
    reference: chr 8
allele count: 2
allele frequency: 1.662786830728301e-5
allele num: 120280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.457C>T
  hgvsp: ENSP00000346119.4:p.Pro153Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.650C>T
  hgvsp: ENSP00000428348.1:p.Pro218Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.665C>T
  hgvsp: ENSP00000428685.1:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1315C>T
  hgvsp: ENSP00000322804.5:p.Pro439Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.487C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.625C>T
  hgvsp: ENSP00000378884.2:p.Pro209Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.576C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1303C>T
  hgvsp: ENSP00000429064.1:p.Pro435Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.973C>T
  hgvsp: ENSP00000428319.1:p.Pro325Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.388C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1228C>T
  hgvsp: ENSP00000367256.3:p.Pro410Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9220G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.457C>T
  hgvsp: ENSP00000393606.2:p.Pro153Ser
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.240C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro435Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

8-125568579-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568579
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568579
    reference: chr 8
allele count: 1
allele frequency: 8.319052293562717e-6
allele num: 120206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.620G>A
  hgvsp: ENSP00000378884.2:p.Arg207Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.968G>A
  hgvsp: ENSP00000428319.1:p.Arg323Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1310G>A
  hgvsp: ENSP00000322804.5:p.Arg437Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.452G>A
  hgvsp: ENSP00000393606.2:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.482G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.660G>A
  hgvsp: ENSP00000428685.1:p.Arg221Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.645G>A
  hgvsp: ENSP00000428348.1:p.Arg216Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.571G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1223G>A
  hgvsp: ENSP00000367256.3:p.Arg408Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.452G>A
  hgvsp: ENSP00000346119.4:p.Arg151Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.383G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.235G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1298G>A
  hgvsp: ENSP00000429064.1:p.Arg433Gln
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9225C>T
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg433Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

8-125568584-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568584
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568584
    reference: chr 8
allele count: 1
allele frequency: 8.328197611472925e-6
allele num: 120074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.447G>A
  hgvsp: ENST00000354184.4:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.566G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1218G>A
  hgvsp: ENST00000378017.3:c.1218G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.963G>A
  hgvsp: ENST00000524090.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.378G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.640G>A
  hgvsp: ENST00000523179.1:c.640G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.615G>A
  hgvsp: ENST00000395508.2:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1293G>A
  hgvsp: ENST00000518547.1:c.1293G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.447G>A
  hgvsp: ENST00000431961.2:c.447G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1305G>A
  hgvsp: ENST00000325064.5:c.1305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9230C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.655G>A
  hgvsp: ENST00000519168.1:c.655G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.477G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.230G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu431Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

8-125568588-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568588
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568588
    reference: chr 8
allele count: 1
allele frequency: 8.329862557267805e-6
allele num: 120050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.611A>G
  hgvsp: ENSP00000378884.2:p.Lys204Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.473A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.443A>G
  hgvsp: ENSP00000346119.4:p.Lys148Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.636A>G
  hgvsp: ENSP00000428348.1:p.Lys213Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.374A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.443A>G
  hgvsp: ENSP00000393606.2:p.Lys148Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1214A>G
  hgvsp: ENSP00000367256.3:p.Lys405Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.226A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.651A>G
  hgvsp: ENSP00000428685.1:p.Lys218Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1301A>G
  hgvsp: ENSP00000322804.5:p.Lys434Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.959A>G
  hgvsp: ENSP00000428319.1:p.Lys320Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1289A>G
  hgvsp: ENSP00000429064.1:p.Lys430Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.562A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9234T>C
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys430Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

8-125568591-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568591
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568591
    reference: chr 8
allele count: 5
allele frequency: 4.169863562064249e-5
allele num: 119908
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.440G>A
  hgvsp: ENSP00000346119.4:p.Arg147His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.470G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.371G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1211G>A
  hgvsp: ENSP00000367256.3:p.Arg404His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9237C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.648G>A
  hgvsp: ENSP00000428685.1:p.Arg217His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.633G>A
  hgvsp: ENSP00000428348.1:p.Arg212His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.956G>A
  hgvsp: ENSP00000428319.1:p.Arg319His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1286G>A
  hgvsp: ENSP00000429064.1:p.Arg429His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.559G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.608G>A
  hgvsp: ENSP00000378884.2:p.Arg203His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.440G>A
  hgvsp: ENSP00000393606.2:p.Arg147His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1298G>A
  hgvsp: ENSP00000322804.5:p.Arg433His
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.223G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37447
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg429His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

8-125568592-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568592
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568592
    reference: chr 8
allele count: 24
allele frequency: 2.00253654629197e-4
allele num: 119848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.607C>T
  hgvsp: ENSP00000378884.2:p.Arg203Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.469C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.439C>T
  hgvsp: ENSP00000393606.2:p.Arg147Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.370C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.647C>T
  hgvsp: ENSP00000428685.1:p.Arg217Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.222C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9238G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.632C>T
  hgvsp: ENSP00000428348.1:p.Arg212Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1297C>T
  hgvsp: ENSP00000322804.5:p.Arg433Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1210C>T
  hgvsp: ENSP00000367256.3:p.Arg404Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.439C>T
  hgvsp: ENSP00000346119.4:p.Arg147Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1285C>T
  hgvsp: ENSP00000429064.1:p.Arg429Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.558C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.955C>T
  hgvsp: ENSP00000428319.1:p.Arg319Cys
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 37478
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16018
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg429Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

8-125568593-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568593
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568593
    reference: chr 8
allele count: 2
allele frequency: 1.667917604870319e-5
allele num: 119910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.606C>T
  hgvsp: ENST00000395508.2:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.221C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9239G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1296C>T
  hgvsp: ENST00000325064.5:c.1296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.369C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1284C>T
  hgvsp: ENST00000518547.1:c.1284C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.631C>T
  hgvsp: ENST00000523179.1:c.631C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.646C>T
  hgvsp: ENST00000519168.1:c.646C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.468C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.438C>T
  hgvsp: ENST00000354184.4:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.438C>T
  hgvsp: ENST00000431961.2:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.954C>T
  hgvsp: ENST00000524090.1:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1209C>T
  hgvsp: ENST00000378017.3:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.557C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.468C>T
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

8-125568595-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568595
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568595
    reference: chr 8
allele count: 10
allele frequency: 8.344180768332165e-5
allele num: 119844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.555C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.604C>T
  hgvsp: ENSP00000378884.2:p.Arg202Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.367C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.952C>T
  hgvsp: ENSP00000428319.1:p.Arg318Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436C>T
  hgvsp: ENSP00000393606.2:p.Arg146Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1294C>T
  hgvsp: ENSP00000322804.5:p.Arg432Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.644C>T
  hgvsp: ENSP00000428685.1:p.Arg216Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436C>T
  hgvsp: ENSP00000346119.4:p.Arg146Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.629C>T
  hgvsp: ENSP00000428348.1:p.Arg211Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9241G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.219C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1282C>T
  hgvsp: ENSP00000429064.1:p.Arg428Cys
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1207C>T
  hgvsp: ENSP00000367256.3:p.Arg403Cys
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg428Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

8-125568598-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568598
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568598
    reference: chr 8
allele count: 1
allele frequency: 8.34432002136146e-6
allele num: 119842
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9244G>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.364C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.216C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-3C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-3C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1279C>G
  hgvsp: ENSP00000429064.1:p.Gln427Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.552C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.626C>G
  hgvsp: ENSP00000428348.1:p.Gln210Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-3C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1291C>G
  hgvsp: ENSP00000322804.5:p.Gln431Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.949C>G
  hgvsp: ENSP00000428319.1:p.Gln317Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.601C>G
  hgvsp: ENSP00000378884.2:p.Gln201Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.641C>G
  hgvsp: ENSP00000428685.1:p.Gln215Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1204C>G
  hgvsp: ENSP00000367256.3:p.Gln402Glu
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37636
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln427Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/8-125568599-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568599
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568599
    reference: chr 8
allele count: 1
allele frequency: 8.349336227769892e-6
allele num: 119770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.625G>T
  hgvsp: ENST00000523179.1:c.625G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.551G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-4G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.600G>T
  hgvsp: ENST00000395508.2:c.600G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1203G>T
  hgvsp: ENST00000378017.3:c.1203G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1290G>T
  hgvsp: ENST00000325064.5:c.1290G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.640G>T
  hgvsp: ENST00000519168.1:c.640G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.948G>T
  hgvsp: ENST00000524090.1:c.948G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-4G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-4G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1278G>T
  hgvsp: ENST00000518547.1:c.1278G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9245C>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.363G>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.215G>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15977
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.466-4G>T
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-125568609-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568609
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568609
    reference: chr 8
allele count: 9
allele frequency: 7.541983709315188e-5
allele num: 119332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.630T>C
  hgvsp: ENSP00000428685.1:p.Val211Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1280T>C
  hgvsp: ENSP00000322804.5:p.Val427Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1193T>C
  hgvsp: ENSP00000367256.3:p.Val398Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1268T>C
  hgvsp: ENSP00000429064.1:p.Val423Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.938T>C
  hgvsp: ENSP00000428319.1:p.Val313Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-14T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-14T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.541T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.590T>C
  hgvsp: ENSP00000378884.2:p.Val197Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9255A>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-14T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.205T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.615T>C
  hgvsp: ENSP00000428348.1:p.Val206Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.353T>C
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15837
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Val423Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

8-125568611-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568611
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568611
    reference: chr 8
allele count: 1
allele frequency: 8.40039649871474e-6
allele num: 119042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1278G>A
  hgvsp: ENST00000325064.5:c.1278G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.351G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1191G>A
  hgvsp: ENST00000378017.3:c.1191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.936G>A
  hgvsp: ENST00000524090.1:c.936G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1266G>A
  hgvsp: ENST00000518547.1:c.1266G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.613G>A
  hgvsp: ENST00000523179.1:c.613G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-16G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-16G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-16G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.203G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9257C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.628G>A
  hgvsp: ENST00000519168.1:c.628G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.588G>A
  hgvsp: ENST00000395508.2:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.539G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15675
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu422Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-125568618-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568618
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568618
    reference: chr 8
allele count: 1
allele frequency: 8.442808415791428e-6
allele num: 118444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1271A>C
  hgvsp: ENSP00000322804.5:p.Gln424Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-23A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.606A>C
  hgvsp: ENSP00000428348.1:p.Gln203Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-23A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.929A>C
  hgvsp: ENSP00000428319.1:p.Gln310Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1259A>C
  hgvsp: ENSP00000429064.1:p.Gln420Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1184A>C
  hgvsp: ENSP00000367256.3:p.Gln395Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.344A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.196A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.581A>C
  hgvsp: ENSP00000378884.2:p.Gln194Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.532A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-23A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9264T>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.621A>C
  hgvsp: ENSP00000428685.1:p.Gln208Pro
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln420Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

8-125568623-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568623
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568623
    reference: chr 8
allele count: 15669
allele frequency: 1.33063283399572e-1
allele num: 117756
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-28T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.601T>C
  hgvsp: ENST00000523179.1:c.601T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.339T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.616T>C
  hgvsp: ENST00000519168.1:c.616T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.527T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-28T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9269A>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.924T>C
  hgvsp: ENST00000524090.1:c.924T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1179T>C
  hgvsp: ENST00000378017.3:c.1179T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.576T>C
  hgvsp: ENST00000395508.2:c.576T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1266T>C
  hgvsp: ENST00000325064.5:c.1266T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1254T>C
  hgvsp: ENST00000518547.1:c.1254T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-28T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.191T>C
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.75e1
  variant carriers: 749
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 4.25e1
  variant carriers: 1733
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 1.75e1
  variant carriers: 672
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 3.25e1
  variant carriers: 1969
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 7.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 4.75e1
  variant carriers: 1383
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.25e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 1.25e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 3.75e1
  variant carriers: 2016
genotype depth: GenotypeDepth
  all individuals: 28981
  bin: 2.25e1
  variant carriers: 1206
genotype quality: GenotypeQuality
hgvs: p.Tyr418Tyr
num of homozygotes: 1153
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

8-125568630-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568630
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568630
    reference: chr 8
allele count: 13
allele frequency: 1.129040662833718e-4
allele num: 115142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-35G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1259G>A
  hgvsp: ENSP00000322804.5:p.Gly420Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.569G>A
  hgvsp: ENSP00000378884.2:p.Gly190Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.520G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.184G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.917G>A
  hgvsp: ENSP00000428319.1:p.Gly306Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-35G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.609G>A
  hgvsp: ENSP00000428685.1:p.Gly204Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.332G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1247G>A
  hgvsp: ENSP00000429064.1:p.Gly416Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.594G>A
  hgvsp: ENSP00000428348.1:p.Gly199Glu
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-35G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9276C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1172G>A
  hgvsp: ENSP00000367256.3:p.Gly391Glu
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17732
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly416Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

8-125568638-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568638
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568638
    reference: chr 8
allele count: 12
allele frequency: 1.055576080646013e-4
allele num: 113682
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.909T>C
  hgvsp: ENST00000524090.1:c.909T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-43T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.176T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.561T>C
  hgvsp: ENST00000395508.2:c.561T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1164T>C
  hgvsp: ENST00000378017.3:c.1164T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.512T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-43T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-43T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.586T>C
  hgvsp: ENST00000523179.1:c.586T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9284A>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.324T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1239T>C
  hgvsp: ENST00000518547.1:c.1239T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.601T>C
  hgvsp: ENST00000519168.1:c.601T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1251T>C
  hgvsp: ENST00000325064.5:c.1251T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala413Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

8-125568645-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568645
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568645
    reference: chr 8
allele count: 1
allele frequency: 8.958967926894822e-6
allele num: 111620
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.505A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1232A>C
  hgvsp: ENSP00000429064.1:p.Asp411Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.317A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-50A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.554A>C
  hgvsp: ENSP00000378884.2:p.Asp185Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-50A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1244A>C
  hgvsp: ENSP00000322804.5:p.Asp415Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.579A>C
  hgvsp: ENSP00000428348.1:p.Asp194Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1157A>C
  hgvsp: ENSP00000367256.3:p.Asp386Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.169A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.902A>C
  hgvsp: ENSP00000428319.1:p.Asp301Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.594A>C
  hgvsp: ENSP00000428685.1:p.Asp199Ala
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-50A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9291T>G
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15449
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp411Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

8-125568646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568646
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568646
    reference: chr 8
allele count: 2
allele frequency: 1.798237727027513e-5
allele num: 111220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1156G>A
  hgvsp: ENSP00000367256.3:p.Asp386Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.901G>A
  hgvsp: ENSP00000428319.1:p.Asp301Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-51G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-51G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.593G>A
  hgvsp: ENSP00000428685.1:p.Asp199Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1231G>A
  hgvsp: ENSP00000429064.1:p.Asp411Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578G>A
  hgvsp: ENSP00000428348.1:p.Asp194Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.316G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-51G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9292C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.168G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.553G>A
  hgvsp: ENSP00000378884.2:p.Asp185Asn
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.504G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1243G>A
  hgvsp: ENSP00000322804.5:p.Asp415Asn
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15234
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp411Asn
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

8-125568650-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568650
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568650
    reference: chr 8
allele count: 1
allele frequency: 9.083972239380837e-6
allele num: 110084
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1156-4A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-55A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.164A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.901-4A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.316-4A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9296T>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.553-4A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-55A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.593-4A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1231-4A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-4A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1243-4A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.504-4A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-55A>G
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25344
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1231-4A>G
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

8-125568663-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568663
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568663
    reference: chr 8
allele count: 1
allele frequency: 9.668187794879727e-6
allele num: 103432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9309C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-68G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-68G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.316-17G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-17G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-68G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.151G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.901-17G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.593-17G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.553-17G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1156-17G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.504-17G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1231-17G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1243-17G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17290
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

8-125568664-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568664
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568664
    reference: chr 8
allele count: 187
allele frequency: 1.809665744091974e-3
allele num: 103334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.553-18C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-69C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.901-18C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1156-18C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1231-18C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.504-18C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-18C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-69C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.150C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-69C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.593-18C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9310G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.316-18C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1243-18C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 2.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 1.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 17315
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP

8-125568666-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568666
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568666
    reference: chr 8
allele count: 2
allele frequency: 1.945336056803813e-5
allele num: 102810
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1231-20A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.901-20A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.148A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9312T>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-71A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.593-20A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-20A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.316-20A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1243-20A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.553-20A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.504-20A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1156-20A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-71A>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-71A>C
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

8-125568672-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568672
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568672
    reference: chr 8
allele count: 2
allele frequency: 1.991238550378335e-5
allele num: 100440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.901-26C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-77C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.504-26C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-26C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-77C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1231-26C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1156-26C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9318G>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.316-26C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.142C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.553-26C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1243-26C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.593-26C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-77C>A
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13481
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

8-125568678-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568678
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568678
    reference: chr 8
allele count: 9
allele frequency: 9.2009487200458e-5
allele num: 97816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.136C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1243-32C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.593-32C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.553-32C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-83C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-83C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9324G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.504-32C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.316-32C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-83C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-32C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.901-32C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1231-32C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1156-32C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20442
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8752
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12011
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

8-125568680-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568680
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568680
    reference: chr 8
allele count: 1
allele frequency: 1.025451711478906e-5
allele num: 97518
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-85G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.593-34G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1231-34G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.134G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.901-34G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-34G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-85G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.504-34G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9326C>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1156-34G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1243-34G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.316-34G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-85G>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.553-34G>C
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

8-125568681-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568681
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568681
    reference: chr 8
allele count: 2
allele frequency: 2.059901948667244e-5
allele num: 97092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-86A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.133A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.504-35A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1243-35A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-86A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.316-35A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.593-35A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-86A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1231-35A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.553-35A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1156-35A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-35A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.901-35A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9327T>C
  variant of: http://identifiers.org/hgnc/7704
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9874
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

8-125568688-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125568688
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125568688
    reference: chr 8
allele count: 7
allele frequency: 7.396449704142012e-5
allele num: 94640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-42G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.553-42G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.593-42G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1243-42G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.901-42G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520771
  gene symbol: MTSS1
  hgvsc: ENST00000520771.1:n.126G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.408+9334C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.466-93G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-93G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1231-42G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.316-42G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.504-42G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1156-42G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-93G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8465
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14711
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19704
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD

8-125569871-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569871
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569871
    reference: chr 8
allele count: 1
allele frequency: 4.665920119447555e-5
allele num: 21432
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1230+51C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1225C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.465+51C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1276C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1242+51C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.900+51C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.315+51C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.503+51C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1276C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1083C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.552+51C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-10017G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.592+51C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32913
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

8-125569874-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569874
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569874
    reference: chr 8
allele count: 5
allele frequency: 2.335139174294788e-4
allele num: 21412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1080C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1230+48C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.503+48C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.315+48C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.552+48C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.592+48C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1242+48C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1228C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1279C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.900+48C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1279C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.465+48C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-10014G>A
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

8-125569891-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569891
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569891
    reference: chr 8
allele count: 1
allele frequency: 4.538440591812653e-5
allele num: 22034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.900+31G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.552+31G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.315+31G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.503+31G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.465+31G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1296G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.592+31G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1230+31G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1245G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1242+31G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9997C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1063G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1296G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16728
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

8-125569892-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569892
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569892
    reference: chr 8
allele count: 4
allele frequency: 1.776041204155936e-4
allele num: 22522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1062C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.592+30C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.315+30C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1297C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.503+30C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1297C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1246C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1242+30C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.900+30C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.552+30C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9996G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1230+30C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.465+30C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17622
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29592
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

8-125569905-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569905
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569905
    reference: chr 8
allele count: 3
allele frequency: 1.227194633068805e-4
allele num: 24446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1242+17C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1259C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1310C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1310C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1230+17C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1049C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9983G>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.315+17C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.552+17C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.465+17C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.900+17C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.592+17C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.503+17C>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23438
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23812
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

8-125569906-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569906
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569906
    reference: chr 8
allele count: 1
allele frequency: 4.055807916937054e-5
allele num: 24656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.900+16C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.592+16C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1260C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1230+16C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9982G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.552+16C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1311C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1048C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.503+16C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1242+16C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.315+16C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1311C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.465+16C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

8-125569909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569909
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569909
    reference: chr 8
allele count: 1
allele frequency: 3.938868756893021e-5
allele num: 25388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1314C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.315+13C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1242+13C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.900+13C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1263C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.465+13C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.592+13C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.503+13C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1314C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1045C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9979G>A
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1230+13C>T
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.552+13C>T
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25946
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21077
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-125569913-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569913
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569913
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 26332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1267C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.315+9C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1242+9C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1318C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.592+9C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.552+9C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.900+9C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1230+9C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.465+9C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9975G>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1318C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.503+9C>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1041C>G
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27835
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18869
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

8-125569917-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569917
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569917
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 27022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1322G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.592+5G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1230+5G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.552+5G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.900+5G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.503+5G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1242+5G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1037G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9971C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.465+5G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.315+5G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1271G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1322G>A
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 16932
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29491
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1230+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

8-125569927-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569927
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569927
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 29404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.460T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.587T>C
  hgvsp: ENSP00000428685.1:p.Trp197Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1027T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.498T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1225T>C
  hgvsp: ENSP00000429064.1:p.Trp409Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1281T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.310T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1237T>C
  hgvsp: ENSP00000322804.5:p.Trp413Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.547T>C
  hgvsp: ENSP00000378884.2:p.Trp183Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1332T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.895T>C
  hgvsp: ENSP00000428319.1:p.Trp299Arg
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1332T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9961A>G
  variant of: http://identifiers.org/hgnc/7704
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32654
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp409Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD

8-125569934-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569934
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569934
    reference: chr 8
allele count: 1
allele frequency: 3.180459258316901e-5
allele num: 31442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.618C>A
  hgvsp: ENST00000522118.1:c.618C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.540C>A
  hgvsp: ENST00000395508.2:c.540C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1339C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1218C>A
  hgvsp: ENST00000518547.1:c.1218C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1020C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.491C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1339C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.453C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.580C>A
  hgvsp: ENST00000519168.1:c.580C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9954G>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1230C>A
  hgvsp: ENST00000325064.5:c.1230C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.303C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1288C>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.888C>A
  hgvsp: ENST00000524090.1:c.888C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile406Ile
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

8-125569936-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569936
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569936
    reference: chr 8
allele count: 1
allele frequency: 3.122658006495129e-5
allele num: 32024
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1216A>G
  hgvsp: ENSP00000429064.1:p.Ile406Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.886A>G
  hgvsp: ENSP00000428319.1:p.Ile296Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.578A>G
  hgvsp: ENSP00000428685.1:p.Ile194Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1018A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1228A>G
  hgvsp: ENSP00000322804.5:p.Ile410Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.489A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1290A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.616A>G
  hgvsp: ENSP00000428145.1:p.Ile206Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.538A>G
  hgvsp: ENSP00000378884.2:p.Ile180Val
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1341A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1341A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9952T>C
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.301A>G
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.451A>G
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9639
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile406Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

8-125569945-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569945
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569945
    reference: chr 8
allele count: 3
allele frequency: 8.578781812982556e-5
allele num: 34970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1009T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9943A>G
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1207T>C
  hgvsp: ENSP00000429064.1:p.Ser403Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1350T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.569T>C
  hgvsp: ENSP00000428685.1:p.Ser191Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.292T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.529T>C
  hgvsp: ENSP00000378884.2:p.Ser177Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.877T>C
  hgvsp: ENSP00000428319.1:p.Ser293Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1350T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.442T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.607T>C
  hgvsp: ENSP00000428145.1:p.Ser203Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1219T>C
  hgvsp: ENSP00000322804.5:p.Ser407Pro
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.480T>C
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1299T>C
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35512
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4155
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser403Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

8-125569946-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 125569946
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 125569946
    reference: chr 8
allele count: 2
allele frequency: 5.688929343497554e-5
allele num: 35156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428348
  ensembl transcript: ENST00000523179
  gene symbol: MTSS1
  hgvsc: ENST00000523179.1:c.578-1300G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428145
  ensembl transcript: ENST00000522118
  gene symbol: MTSS1
  hgvsc: ENST00000522118.1:c.606G>A
  hgvsp: ENST00000522118.1:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000346119
  ensembl transcript: ENST00000354184
  gene symbol: MTSS1
  hgvsc: ENST00000354184.4:c.436-1351G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147684
  ensembl protein: ENSP00000431115
  ensembl transcript: ENST00000522532
  gene symbol: NDUFB9
  hgvsc: ENST00000522532.1:c.409-9942C>T
  variant of: http://identifiers.org/hgnc/7704
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000429064
  ensembl transcript: ENST00000518547
  gene symbol: MTSS1
  hgvsc: ENST00000518547.1:c.1206G>A
  hgvsp: ENST00000518547.1:c.1206G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000322804
  ensembl transcript: ENST00000325064
  gene symbol: MTSS1
  hgvsc: ENST00000325064.5:c.1218G>A
  hgvsp: ENST00000325064.5:c.1218G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000523587
  gene symbol: MTSS1
  hgvsc: ENST00000523587.1:n.479G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000378884
  ensembl transcript: ENST00000395508
  gene symbol: MTSS1
  hgvsc: ENST00000395508.2:c.528G>A
  hgvsp: ENST00000395508.2:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000522722
  gene symbol: MTSS1
  hgvsc: ENST00000522722.1:n.441G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428319
  ensembl transcript: ENST00000524090
  gene symbol: MTSS1
  hgvsc: ENST00000524090.1:c.876G>A
  hgvsp: ENST00000524090.1:c.876G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000393606
  ensembl transcript: ENST00000431961
  gene symbol: MTSS1
  hgvsc: ENST00000431961.2:c.436-1351G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000170873
  ensembl transcript: ENST00000520094
  gene symbol: MTSS1
  hgvsc: ENST00000520094.1:n.291G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000367256
  ensembl transcript: ENST00000378017
  gene symbol: MTSS1
  hgvsc: ENST00000378017.3:c.1155+1008G>A
  variant of: http://identifiers.org/hgnc/20443
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000170873
  ensembl protein: ENSP00000428685
  ensembl transcript: ENST00000519168
  gene symbol: MTSS1
  hgvsc: ENST00000519168.1:c.568G>A
  hgvsp: ENST00000519168.1:c.568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20443
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro402Pro
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

5-140783805-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140783805
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 140783805
    reference: chr 5
allele count: 1
allele frequency: 8.340005337603416e-6
allele num: 119904
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204956
  ensembl protein: ENSP00000431083
  ensembl transcript: ENST00000517417
  gene symbol: PCDHGA1
  hgvsc: ENST00000517417.1:c.2421+71133C>T
  variant of: http://identifiers.org/hgnc/8696
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000081853
  ensembl protein: ENSP00000378077
  ensembl transcript: ENST00000394576
  gene symbol: PCDHGA2
  hgvsc: ENST00000394576.2:c.2424+62843C>T
  variant of: http://identifiers.org/hgnc/8700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254245
  ensembl protein: ENSP00000253812
  ensembl transcript: ENST00000253812
  gene symbol: PCDHGA3
  hgvsc: ENST00000253812.6:c.2424+57781C>T
  variant of: http://identifiers.org/hgnc/8701
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253537
  ensembl protein: ENSP00000430024
  ensembl transcript: ENST00000518325
  gene symbol: PCDHGA7
  hgvsc: ENST00000518325.1:c.2424+18915C>T
  variant of: http://identifiers.org/hgnc/8705
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262209
  ensembl protein: ENSP00000461862
  ensembl transcript: ENST00000576222
  gene symbol: PCDHGB3
  hgvsc: ENST00000576222.1:c.2415+31429C>T
  variant of: http://identifiers.org/hgnc/8710
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254221
  ensembl protein: ENSP00000429273
  ensembl transcript: ENST00000523390
  gene symbol: PCDHGB1
  hgvsc: ENST00000523390.1:c.2409+51569C>T
  variant of: http://identifiers.org/hgnc/8708
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253485
  ensembl protein: ENSP00000429834
  ensembl transcript: ENST00000518069
  gene symbol: PCDHGA5
  hgvsc: ENST00000518069.1:c.2421+37487C>T
  variant of: http://identifiers.org/hgnc/8703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253731
  ensembl protein: ENSP00000429601
  ensembl transcript: ENST00000517434
  gene symbol: PCDHGA6
  hgvsc: ENST00000517434.1:c.2424+27731C>T
  variant of: http://identifiers.org/hgnc/8704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262576
  ensembl protein: ENSP00000458570
  ensembl transcript: ENST00000571252
  gene symbol: PCDHGA4
  hgvsc: ENST00000571252.1:c.2421+46617C>T
  variant of: http://identifiers.org/hgnc/8702
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253953
  ensembl protein: ENSP00000428288
  ensembl transcript: ENST00000519479
  gene symbol: PCDHGB4
  hgvsc: ENST00000519479.1:c.2397+13957C>T
  variant of: http://identifiers.org/hgnc/8711
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000261934
  ensembl protein: ENSP00000460274
  ensembl transcript: ENST00000573521
  gene symbol: PCDHGA9
  hgvsc: ENST00000573521.1:c.1286C>T
  hgvsp: ENSP00000460274.1:p.Thr429Ile
  variant of: http://identifiers.org/hgnc/8707
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253767
  ensembl protein: ENSP00000381605
  ensembl transcript: ENST00000398604
  gene symbol: PCDHGA8
  hgvsc: ENST00000398604.2:c.2424+9001C>T
  variant of: http://identifiers.org/hgnc/8706
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253910
  ensembl protein: ENSP00000429018
  ensembl transcript: ENST00000522605
  gene symbol: PCDHGB2
  hgvsc: ENST00000522605.1:c.2421+41682C>T
  variant of: http://identifiers.org/hgnc/8709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr429Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

5-140783809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140783809
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 140783809
    reference: chr 5
allele count: 2
allele frequency: 1.665667266306883e-5
allele num: 120072
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253731
  ensembl protein: ENSP00000429601
  ensembl transcript: ENST00000517434
  gene symbol: PCDHGA6
  hgvsc: ENST00000517434.1:c.2424+27735G>A
  variant of: http://identifiers.org/hgnc/8704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253485
  ensembl protein: ENSP00000429834
  ensembl transcript: ENST00000518069
  gene symbol: PCDHGA5
  hgvsc: ENST00000518069.1:c.2421+37491G>A
  variant of: http://identifiers.org/hgnc/8703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253910
  ensembl protein: ENSP00000429018
  ensembl transcript: ENST00000522605
  gene symbol: PCDHGB2
  hgvsc: ENST00000522605.1:c.2421+41686G>A
  variant of: http://identifiers.org/hgnc/8709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000081853
  ensembl protein: ENSP00000378077
  ensembl transcript: ENST00000394576
  gene symbol: PCDHGA2
  hgvsc: ENST00000394576.2:c.2424+62847G>A
  variant of: http://identifiers.org/hgnc/8700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253953
  ensembl protein: ENSP00000428288
  ensembl transcript: ENST00000519479
  gene symbol: PCDHGB4
  hgvsc: ENST00000519479.1:c.2397+13961G>A
  variant of: http://identifiers.org/hgnc/8711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204956
  ensembl protein: ENSP00000431083
  ensembl transcript: ENST00000517417
  gene symbol: PCDHGA1
  hgvsc: ENST00000517417.1:c.2421+71137G>A
  variant of: http://identifiers.org/hgnc/8696
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254245
  ensembl protein: ENSP00000253812
  ensembl transcript: ENST00000253812
  gene symbol: PCDHGA3
  hgvsc: ENST00000253812.6:c.2424+57785G>A
  variant of: http://identifiers.org/hgnc/8701
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262576
  ensembl protein: ENSP00000458570
  ensembl transcript: ENST00000571252
  gene symbol: PCDHGA4
  hgvsc: ENST00000571252.1:c.2421+46621G>A
  variant of: http://identifiers.org/hgnc/8702
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254221
  ensembl protein: ENSP00000429273
  ensembl transcript: ENST00000523390
  gene symbol: PCDHGB1
  hgvsc: ENST00000523390.1:c.2409+51573G>A
  variant of: http://identifiers.org/hgnc/8708
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262209
  ensembl protein: ENSP00000461862
  ensembl transcript: ENST00000576222
  gene symbol: PCDHGB3
  hgvsc: ENST00000576222.1:c.2415+31433G>A
  variant of: http://identifiers.org/hgnc/8710
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253767
  ensembl protein: ENSP00000381605
  ensembl transcript: ENST00000398604
  gene symbol: PCDHGA8
  hgvsc: ENST00000398604.2:c.2424+9005G>A
  variant of: http://identifiers.org/hgnc/8706
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000261934
  ensembl protein: ENSP00000460274
  ensembl transcript: ENST00000573521
  gene symbol: PCDHGA9
  hgvsc: ENST00000573521.1:c.1290G>A
  hgvsp: ENST00000573521.1:c.1290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8707
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253537
  ensembl protein: ENSP00000430024
  ensembl transcript: ENST00000518325
  gene symbol: PCDHGA7
  hgvsc: ENST00000518325.1:c.2424+18919G>A
  variant of: http://identifiers.org/hgnc/8705
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro430Pro
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

5-140783809-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140783809
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 140783809
    reference: chr 5
allele count: 1
allele frequency: 8.328336331534413e-6
allele num: 120072
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253485
  ensembl protein: ENSP00000429834
  ensembl transcript: ENST00000518069
  gene symbol: PCDHGA5
  hgvsc: ENST00000518069.1:c.2421+37491G>T
  variant of: http://identifiers.org/hgnc/8703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253731
  ensembl protein: ENSP00000429601
  ensembl transcript: ENST00000517434
  gene symbol: PCDHGA6
  hgvsc: ENST00000517434.1:c.2424+27735G>T
  variant of: http://identifiers.org/hgnc/8704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253767
  ensembl protein: ENSP00000381605
  ensembl transcript: ENST00000398604
  gene symbol: PCDHGA8
  hgvsc: ENST00000398604.2:c.2424+9005G>T
  variant of: http://identifiers.org/hgnc/8706
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204956
  ensembl protein: ENSP00000431083
  ensembl transcript: ENST00000517417
  gene symbol: PCDHGA1
  hgvsc: ENST00000517417.1:c.2421+71137G>T
  variant of: http://identifiers.org/hgnc/8696
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000261934
  ensembl protein: ENSP00000460274
  ensembl transcript: ENST00000573521
  gene symbol: PCDHGA9
  hgvsc: ENST00000573521.1:c.1290G>T
  hgvsp: ENST00000573521.1:c.1290G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8707
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262209
  ensembl protein: ENSP00000461862
  ensembl transcript: ENST00000576222
  gene symbol: PCDHGB3
  hgvsc: ENST00000576222.1:c.2415+31433G>T
  variant of: http://identifiers.org/hgnc/8710
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253537
  ensembl protein: ENSP00000430024
  ensembl transcript: ENST00000518325
  gene symbol: PCDHGA7
  hgvsc: ENST00000518325.1:c.2424+18919G>T
  variant of: http://identifiers.org/hgnc/8705
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000081853
  ensembl protein: ENSP00000378077
  ensembl transcript: ENST00000394576
  gene symbol: PCDHGA2
  hgvsc: ENST00000394576.2:c.2424+62847G>T
  variant of: http://identifiers.org/hgnc/8700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254245
  ensembl protein: ENSP00000253812
  ensembl transcript: ENST00000253812
  gene symbol: PCDHGA3
  hgvsc: ENST00000253812.6:c.2424+57785G>T
  variant of: http://identifiers.org/hgnc/8701
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253910
  ensembl protein: ENSP00000429018
  ensembl transcript: ENST00000522605
  gene symbol: PCDHGB2
  hgvsc: ENST00000522605.1:c.2421+41686G>T
  variant of: http://identifiers.org/hgnc/8709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254221
  ensembl protein: ENSP00000429273
  ensembl transcript: ENST00000523390
  gene symbol: PCDHGB1
  hgvsc: ENST00000523390.1:c.2409+51573G>T
  variant of: http://identifiers.org/hgnc/8708
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262576
  ensembl protein: ENSP00000458570
  ensembl transcript: ENST00000571252
  gene symbol: PCDHGA4
  hgvsc: ENST00000571252.1:c.2421+46621G>T
  variant of: http://identifiers.org/hgnc/8702
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253953
  ensembl protein: ENSP00000428288
  ensembl transcript: ENST00000519479
  gene symbol: PCDHGB4
  hgvsc: ENST00000519479.1:c.2397+13961G>T
  variant of: http://identifiers.org/hgnc/8711
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28287
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro430Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

5-140783812-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140783812
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 140783812
    reference: chr 5
allele count: 1
allele frequency: 8.315040244794785e-6
allele num: 120264
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000081853
  ensembl protein: ENSP00000378077
  ensembl transcript: ENST00000394576
  gene symbol: PCDHGA2
  hgvsc: ENST00000394576.2:c.2424+62850C>G
  variant of: http://identifiers.org/hgnc/8700
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254245
  ensembl protein: ENSP00000253812
  ensembl transcript: ENST00000253812
  gene symbol: PCDHGA3
  hgvsc: ENST00000253812.6:c.2424+57788C>G
  variant of: http://identifiers.org/hgnc/8701
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000261934
  ensembl protein: ENSP00000460274
  ensembl transcript: ENST00000573521
  gene symbol: PCDHGA9
  hgvsc: ENST00000573521.1:c.1293C>G
  hgvsp: ENST00000573521.1:c.1293C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8707
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253910
  ensembl protein: ENSP00000429018
  ensembl transcript: ENST00000522605
  gene symbol: PCDHGB2
  hgvsc: ENST00000522605.1:c.2421+41689C>G
  variant of: http://identifiers.org/hgnc/8709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262576
  ensembl protein: ENSP00000458570
  ensembl transcript: ENST00000571252
  gene symbol: PCDHGA4
  hgvsc: ENST00000571252.1:c.2421+46624C>G
  variant of: http://identifiers.org/hgnc/8702
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000262209
  ensembl protein: ENSP00000461862
  ensembl transcript: ENST00000576222
  gene symbol: PCDHGB3
  hgvsc: ENST00000576222.1:c.2415+31436C>G
  variant of: http://identifiers.org/hgnc/8710
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253953
  ensembl protein: ENSP00000428288
  ensembl transcript: ENST00000519479
  gene symbol: PCDHGB4
  hgvsc: ENST00000519479.1:c.2397+13964C>G
  variant of: http://identifiers.org/hgnc/8711
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254221
  ensembl protein: ENSP00000429273
  ensembl transcript: ENST00000523390
  gene symbol: PCDHGB1
  hgvsc: ENST00000523390.1:c.2409+51576C>G
  variant of: http://identifiers.org/hgnc/8708
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253537
  ensembl protein: ENSP00000430024
  ensembl transcript: ENST00000518325
  gene symbol: PCDHGA7
  hgvsc: ENST00000518325.1:c.2424+18922C>G
  variant of: http://identifiers.org/hgnc/8705
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253767
  ensembl protein: ENSP00000381605
  ensembl transcript: ENST00000398604
  gene symbol: PCDHGA8
  hgvsc: ENST00000398604.2:c.2424+9008C>G
  variant of: http://identifiers.org/hgnc/8706
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253731
  ensembl protein: ENSP00000429601
  ensembl transcript: ENST00000517434
  gene symbol: PCDHGA6
  hgvsc: ENST00000517434.1:c.2424+27738C>G
  variant of: http://identifiers.org/hgnc/8704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204956
  ensembl protein: ENSP00000431083
  ensembl transcript: ENST00000517417
  gene symbol: PCDHGA1
  hgvsc: ENST00000517417.1:c.2421+71140C>G
  variant of: http://identifiers.org/hgnc/8696
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253485
  ensembl protein: ENSP00000429834
  ensembl transcript: ENST00000518069
  gene symbol: PCDHGA5
  hgvsc: ENST00000518069.1:c.2421+37494C>G
  variant of: http://identifiers.org/hgnc/8703
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7524
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro431Pro
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

5-140783813-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 140783813
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 140783812
    reference: chr 5
allele count: 3
allele frequency: 2.493641214902e-5
allele num: 120306
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254245
  ensembl protein: ENSP00000253812
  ensembl transcript: ENST00000253812
  gene symbol: PCDHGA3
  hgvsc: ENST00000253812.6:c.2424+57790delT
  variant of: http://identifiers.org/hgnc/8701
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253485
  ensembl protein: ENSP00000429834
  ensembl transcript: ENST00000518069
  gene symbol: PCDHGA5
  hgvsc: ENST00000518069.1:c.2421+37496delT
  variant of: http://identifiers.org/hgnc/8703
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000253731
  ensembl protein: ENSP00000429601
  ensembl transcript: ENST00000517434
  gene symbol: PCDHGA6
  hgvsc: ENST00000517434.1:c.2424+27740delT
  variant of: http://identifiers.org/hgnc/8704
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000204956
  ensembl protein: ENSP00000431083
  ensembl transcript: ENST00000517417
  gene symbol: PCDHGA1
  hgvsc: ENST00000517417.1:c.2421+71142delT
  variant of: http://identifiers.org/hgnc/8696
canonical: true
consequence: frameshift
filter: PASS
hgvs: p.Leu432ArgfsTer11
num of homozygotes: 0
reference allele: CT

GenotypeDepth
all individuals: 6
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40194
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49441
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1220
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5135
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.13421666053245e-5
allele num: 16302
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 1.429624e6

QD
type: SiteQuality
SIO_000300: 1.254e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.417e0

GenotypeDepth
all individuals: 3426
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 10
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 555
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 537
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 38
bin: 5.25e1
variant carriers: 5

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

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1206
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 9.75e1
variant carriers: 64

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

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 138
bin: 5.75e1
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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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allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

African
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allele frequency: 9.737098344693281e-5
allele num: 10270
num of homozygotes: 0

European (Non-Finnish)
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allele count: 59
allele frequency: 8.893846664053785e-4
allele num: 66338
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.129704548240775e-5
allele num: 16314
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.745200698080279e-4
allele num: 11460
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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ClippingRankSum
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QD
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InbreedingCoeff
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VQSLOD
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MQRankSum
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SIO_000300: 9.8e-2

BaseQRankSum
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SIO_000300: 3.47e-1

ReadPosRankSum
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SIO_000300: 4.49e-1

FS
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SIO_000300: 5.25e-1

MQ
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SIO_000300: 5.959e1

DP
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SIO_000300: 1.432587e6

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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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: 4

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

East Asian
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allele count: 4
allele frequency: 4.631773969430292e-4
allele num: 8636
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66350
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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SIO_000300: -2.0e-4

QD
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ClippingRankSum
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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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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

Other
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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
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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

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: 6.12369871402327e-5
allele num: 16330
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66358
num of homozygotes: 0

DP
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SIO_000300: 1.430202e6

VQSLOD
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FS
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SIO_000300: 1.2659e1

BaseQRankSum
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -1.296e0

MQRankSum
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SIO_000300: -1.817e0

InbreedingCoeff
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SIO_000300: 0.0e0

QD
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SIO_000300: 1.003e1

ReadPosRankSum
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SIO_000300: 5.05e-1

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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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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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66378
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 2
allele frequency: 1.223840411210378e-4
allele num: 16342
num of homozygotes: 0

ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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SIO_000300: 6.882e0

InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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SIO_000300: 1.03e0

MQ
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SIO_000300: 5.955e1

QD
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SIO_000300: 1.234e1

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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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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Other
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East Asian
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African
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
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QD
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ReadPosRankSum
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FS
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MQ
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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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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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African
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num of homozygotes: 0

Latino
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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QD
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MQRankSum
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FS
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DP
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ClippingRankSum
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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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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Latino
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South Asian
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.012320390396723e-5
allele num: 66394
num of homozygotes: 0

African
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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
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.415e1

VQSLOD
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SIO_000300: 5.610000000000001e-1

DP
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SIO_000300: 1.43071e6

ReadPosRankSum
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SIO_000300: 7.000000000000001e-2

ClippingRankSum
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

MQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

FS
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SIO_000300: 2.679e0

GenotypeDepth
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variant carriers: 1

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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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: 1

African
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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

South Asian
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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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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

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

Other
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ClippingRankSum
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FS
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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ReadPosRankSum
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MQ
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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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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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6396
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: 4.886988393402566e-4
allele num: 16370
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.536249359418804e-5
allele num: 66346
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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African
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East Asian
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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SIO_000300: -1.043e0

ReadPosRankSum
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SIO_000300: 2.4e-2

DP
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SIO_000300: 1.427158e6

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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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: 66360
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6396
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African
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allele count: 3
allele frequency: 2.918287937743191e-4
allele num: 10280
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South Asian
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allele count: 0
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Other
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ClippingRankSum
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SIO_000300: -7.41e-1

BaseQRankSum
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MQ
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VQSLOD
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DP
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QD
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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SIO_000300: -3.0e-4

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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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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allele frequency: 0.0e0
allele num: 6390
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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African
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Other
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.522022248349462e-5
allele num: 66342
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South Asian
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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FS
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MQ
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BaseQRankSum
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DP
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VQSLOD
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ClippingRankSum
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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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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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South Asian
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East Asian
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African
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Latino
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Other
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European (Finnish)
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European (Non-Finnish)
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ClippingRankSum
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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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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African
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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FS
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DP
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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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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.507113576079093e-5
allele num: 66352
num of homozygotes: 0

African
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South Asian
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Other
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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QD
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MQRankSum
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ReadPosRankSum
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DP
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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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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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East Asian
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Latino
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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FS
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DP
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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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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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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African
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Other
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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South Asian
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InbreedingCoeff
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FS
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VQSLOD
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QD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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DP
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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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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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Other
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Latino
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African
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European (Non-Finnish)
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East Asian
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European (Finnish)
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DP
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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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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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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East Asian
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African
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European (Non-Finnish)
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Latino
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South Asian
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ReadPosRankSum
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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FS
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ClippingRankSum
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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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South Asian
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East Asian
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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Latino
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FS
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QD
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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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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South Asian
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African
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European (Non-Finnish)
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allele num: 66294
num of homozygotes: 0

East Asian
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Other
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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ClippingRankSum
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DP
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BaseQRankSum
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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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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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East Asian
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allele frequency: 0.0e0
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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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num of homozygotes: 0

African
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Other
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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MQ
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QD
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ReadPosRankSum
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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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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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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Other
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African
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European (Non-Finnish)
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num of homozygotes: 0

Latino
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South Asian
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VQSLOD
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ReadPosRankSum
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QD
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MQ
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ClippingRankSum
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MQRankSum
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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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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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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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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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: 1
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allele num: 66218
num of homozygotes: 0

South Asian
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East Asian
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African
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Latino
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BaseQRankSum
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SIO_000300: 2.3e0

FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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ClippingRankSum
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DP
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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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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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East Asian
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European (Finnish)
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Latino
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African
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South Asian
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European (Non-Finnish)
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Other
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VQSLOD
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QD
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ClippingRankSum
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BaseQRankSum
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FS
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DP
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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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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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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European (Non-Finnish)
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allele num: 66140
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East Asian
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European (Finnish)
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African
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Other
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Latino
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South Asian
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DP
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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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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Latino
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European (Finnish)
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Other
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African
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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MQ
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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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QD
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DP
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MQRankSum
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ClippingRankSum
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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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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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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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MQ
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InbreedingCoeff
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DP
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ReadPosRankSum
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QD
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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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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European (Non-Finnish)
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allele num: 66148
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Other
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African
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allele frequency: 0.0e0
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Latino
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South Asian
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East Asian
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European (Finnish)
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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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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East Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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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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European (Finnish)
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African
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South Asian
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East Asian
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European (Non-Finnish)
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Other
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DP
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MQRankSum
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ReadPosRankSum
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QD
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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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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European (Non-Finnish)
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Other
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Latino
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East Asian
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South Asian
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African
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European (Finnish)
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MQRankSum
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MQ
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FS
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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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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East Asian
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522858100082234e-5
allele num: 65666
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.603e-1

DP
type: SiteQuality
SIO_000300: 1.400131e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.386e0

QD
type: SiteQuality
SIO_000300: 1.406e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
all individuals: 13225
bin: 2.75e1
variant carriers: 1677

GenotypeDepth
all individuals: 1082
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variant carriers: 1046

GenotypeDepth
all individuals: 88
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variant carriers: 87

GenotypeDepth
all individuals: 342
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variant carriers: 339

GenotypeDepth
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variant carriers: 161

GenotypeDepth
all individuals: 343
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variant carriers: 342

GenotypeDepth
all individuals: 553
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variant carriers: 545

GenotypeQuality
all individuals: 3214
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variant carriers: 11

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 304
bin: 5.75e1
variant carriers: 37

GenotypeQuality
all individuals: 2649
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variant carriers: 54

GenotypeQuality
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bin: 4.25e1
variant carriers: 18

GenotypeQuality
all individuals: 116
bin: 8.75e1
variant carriers: 52

GenotypeQuality
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bin: 6.25e1
variant carriers: 50

GenotypeQuality
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variant carriers: 52

GenotypeQuality
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bin: 2.5e0
variant carriers: 4

GenotypeQuality
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variant carriers: 13947

GenotypeQuality
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bin: 8.25e1
variant carriers: 83

GenotypeQuality
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bin: 4.75e1
variant carriers: 36

GenotypeQuality
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bin: 7.5e0
variant carriers: 7

GenotypeQuality
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variant carriers: 67

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 61

GenotypeQuality
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variant carriers: 38

GenotypeQuality
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bin: 3.75e1
variant carriers: 15

GenotypeQuality
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bin: 3.25e1
variant carriers: 8

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 516
bin: 2.75e1
variant carriers: 13

Latino
type: Population
allele count: 2334
allele frequency: 2.049525816649104e-1
allele num: 11388
num of homozygotes: 247

European (Finnish)
type: Population
allele count: 644
allele frequency: 1.049543676662321e-1
allele num: 6136
num of homozygotes: 36

East Asian
type: Population
allele count: 1163
allele frequency: 1.357693205696942e-1
allele num: 8566
num of homozygotes: 82

African
type: Population
allele count: 1558
allele frequency: 1.536489151873767e-1
allele num: 10140
num of homozygotes: 131

European (Non-Finnish)
type: Population
allele count: 8942
allele frequency: 1.367445559089797e-1
allele num: 65392
num of homozygotes: 612

South Asian
type: Population
allele count: 881
allele frequency: 5.771750524109015e-2
allele num: 15264
num of homozygotes: 33

Other
type: Population
allele count: 147
allele frequency: 1.689655172413793e-1
allele num: 870
num of homozygotes: 12

VQSLOD
type: SiteQuality
SIO_000300: 4.65e0

FS
type: SiteQuality
SIO_000300: 5.55e-1

DP
type: SiteQuality
SIO_000300: 1.652533e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

QD
type: SiteQuality
SIO_000300: 1.483e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.76e-2

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.87e-1

GenotypeDepth
all individuals: 17
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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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variant carriers: 13

GenotypeQuality
all individuals: 472
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variant carriers: 0

GenotypeQuality
all individuals: 15
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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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GenotypeQuality
all individuals: 887
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 43999
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variant carriers: 0

GenotypeQuality
all individuals: 248
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variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.864685955806943e-4
allele num: 64354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.007252215954875e-4
allele num: 9928
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.37974e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 1.202e1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeDepth
all individuals: 5894
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3650
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variant carriers: 0

GenotypeDepth
all individuals: 1394
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variant carriers: 0

GenotypeDepth
all individuals: 70
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variant carriers: 0

GenotypeDepth
all individuals: 6
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variant carriers: 1

GenotypeDepth
all individuals: 16569
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variant carriers: 0

GenotypeDepth
all individuals: 28796
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variant carriers: 1

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 105
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variant carriers: 0

GenotypeQuality
all individuals: 235
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GenotypeQuality
all individuals: 1083
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variant carriers: 0

GenotypeQuality
all individuals: 172
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variant carriers: 0

GenotypeQuality
all individuals: 42660
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variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 411
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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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variant carriers: 0

GenotypeQuality
all individuals: 536
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GenotypeQuality
all individuals: 280
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variant carriers: 0

GenotypeQuality
all individuals: 1090
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variant carriers: 0

GenotypeQuality
all individuals: 3725
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 675
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variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.75e1
variant carriers: 12

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.881644557343118e-4
allele num: 63774
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.344854e6

FS
type: SiteQuality
SIO_000300: 1.907e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 1.327e1

GenotypeDepth
all individuals: 18
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3056
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 27114
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variant carriers: 0

GenotypeDepth
all individuals: 439
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variant carriers: 0

GenotypeDepth
all individuals: 7737
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variant carriers: 0

GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeDepth
all individuals: 40
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variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 286
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variant carriers: 0

GenotypeQuality
all individuals: 167
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GenotypeQuality
all individuals: 314
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variant carriers: 0

GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 235
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GenotypeQuality
all individuals: 68
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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
all individuals: 21
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GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 666
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GenotypeQuality
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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: 3381
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GenotypeQuality
all individuals: 590
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.589875671722471e-5
allele num: 62898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5686
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.301195e6

VQSLOD
type: SiteQuality
SIO_000300: -5.349e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

QD
type: SiteQuality
SIO_000300: 9.25e0

FS
type: SiteQuality
SIO_000300: 6.143e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.21e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

GenotypeDepth
all individuals: 1660
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8137
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
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variant carriers: 0

GenotypeDepth
all individuals: 26721
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variant carriers: 1

GenotypeDepth
all individuals: 17
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variant carriers: 0

GenotypeDepth
all individuals: 11
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GenotypeDepth
all individuals: 18
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GenotypeDepth
all individuals: 4
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GenotypeDepth
all individuals: 12
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GenotypeQuality
all individuals: 1526
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GenotypeQuality
all individuals: 309
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GenotypeQuality
all individuals: 236
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GenotypeQuality
all individuals: 53
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GenotypeQuality
all individuals: 10231
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GenotypeQuality
all individuals: 321
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GenotypeQuality
all individuals: 372
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GenotypeQuality
all individuals: 114
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 3336
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11028
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.063557573256294e-4
allele num: 9692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13022
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5658
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

QD
type: SiteQuality
SIO_000300: 1.157e1

DP
type: SiteQuality
SIO_000300: 1.293772e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 2.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.107e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 14496
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 17
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GenotypeDepth
all individuals: 4
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GenotypeDepth
all individuals: 12
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GenotypeDepth
all individuals: 2908
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GenotypeQuality
all individuals: 222
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GenotypeQuality
all individuals: 38
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GenotypeQuality
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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: 413
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 238
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GenotypeQuality
all individuals: 128
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GenotypeQuality
all individuals: 212
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GenotypeQuality
all individuals: 37605
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GenotypeQuality
all individuals: 548
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GenotypeQuality
all individuals: 424
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GenotypeQuality
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GenotypeQuality
all individuals: 1843
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variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.6069936363052e-5
allele num: 62228
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.395e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e-1

QD
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SIO_000300: 1.522e1

InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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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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allele frequency: 0.0e0
allele num: 10462
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.683728448275862e-5
allele num: 59392
num of homozygotes: 0

African
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South Asian
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Other
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DP
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQ
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MQRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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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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East Asian
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allele frequency: 0.0e0
allele num: 7828
num of homozygotes: 0

Other
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South Asian
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European (Non-Finnish)
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allele num: 59318
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European (Finnish)
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African
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allele frequency: 1.718547341115435e-2
allele num: 9252
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Latino
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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VQSLOD
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MQ
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DP
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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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African
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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

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

European (Non-Finnish)
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European (Finnish)
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South Asian
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Other
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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BaseQRankSum
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VQSLOD
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QD
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FS
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MQ
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ClippingRankSum
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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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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 2.289901534234028e-4
allele num: 8734
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 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

South Asian
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num of homozygotes: 0

East Asian
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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FS
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MQ
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 5
allele frequency: 5.857544517338331e-4
allele num: 8536
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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.803036313151347e-5
allele num: 55462
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 1.216249087813184e-4
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FS
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MQRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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InbreedingCoeff
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QD
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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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allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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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: 1
allele frequency: 1.013376570733685e-4
allele num: 9868
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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MQRankSum
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SIO_000300: 3.79e-1

FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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QD
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BaseQRankSum
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DP
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ReadPosRankSum
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SIO_000300: -3.31e-1

GenotypeDepth
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variant carriers: 0

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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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6976
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9858
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 1.693766937669377e-3
allele num: 2952
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
allele num: 730
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

BaseQRankSum
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SIO_000300: -2.925e0

ReadPosRankSum
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FS
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SIO_000300: 0.0e0

MQRankSum
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DP
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MQ
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -5.37e-2

VQSLOD
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QD
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SIO_000300: 1.475e1

GenotypeDepth
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variant carriers: 0

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: 10136
num of homozygotes: 0

East Asian
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
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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 (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 1.383125864453665e-4
allele num: 7230
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FS
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SIO_000300: 4.961e0

VQSLOD
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MQRankSum
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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DP
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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: 2

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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African
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East Asian
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allele frequency: 3.989361702127659e-3
allele num: 752
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European (Non-Finnish)
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European (Finnish)
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Other
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DP
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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QD
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MQ
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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: 5

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele num: 3134
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East Asian
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South Asian
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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allele frequency: 1.739130434782609e-4
allele num: 11500
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Other
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FS
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VQSLOD
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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Other
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African
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DP
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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VQSLOD
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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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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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 13042
num of homozygotes: 0

Other
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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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allele frequency: 0.0e0
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European (Finnish)
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VQSLOD
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FS
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ClippingRankSum
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QD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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Other
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ReadPosRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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DP
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FS
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VQSLOD
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QD
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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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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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African
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Latino
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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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South Asian
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MQ
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DP
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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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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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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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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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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African
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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MQ
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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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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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South Asian
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FS
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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MQ
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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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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Latino
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South Asian
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European (Finnish)
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African
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East Asian
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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MQ
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QD
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DP
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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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South Asian
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European (Finnish)
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European (Non-Finnish)
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African
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East Asian
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Latino
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MQRankSum
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
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VQSLOD
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ClippingRankSum
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DP
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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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European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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South Asian
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Latino
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Other
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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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VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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MQ
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QD
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FS
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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DP
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