17-1372853-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372853
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372853
    reference: chr 17
allele count: 1
allele frequency: 9.485146260955344e-6
allele num: 105428
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2582G>A
  hgvsp: ENSP00000352834.5:p.Arg861Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2477G>A
  hgvsp: ENSP00000354283.2:p.Arg826Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.101G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.266G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2477G>A
  hgvsp: ENSP00000459174.1:p.Arg826Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2525G>A
  hgvsp: ENSP00000412197.2:p.Arg842Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2510G>A
  hgvsp: ENSP00000437685.2:p.Arg837Gln
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8771
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg861Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

17-1372854-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372854
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372854
    reference: chr 17
allele count: 1
allele frequency: 9.450366674226959e-6
allele num: 105816
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2581C>T
  hgvsp: ENSP00000352834.5:p.Arg861Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.265C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2476C>T
  hgvsp: ENSP00000459174.1:p.Arg826Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2509C>T
  hgvsp: ENSP00000437685.2:p.Arg837Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2524C>T
  hgvsp: ENSP00000412197.2:p.Arg842Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.100C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2476C>T
  hgvsp: ENSP00000354283.2:p.Arg826Trp
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8632
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6866
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg861Trp
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-1372861-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372861
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372861
    reference: chr 17
allele count: 838
allele frequency: 7.805077957640221e-3
allele num: 107366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2469A>C
  hgvsp: ENSP00000459174.1:p.Lys823Asn
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2502A>C
  hgvsp: ENSP00000437685.2:p.Lys834Asn
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.258A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2574A>C
  hgvsp: ENSP00000352834.5:p.Lys858Asn
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2469A>C
  hgvsp: ENSP00000354283.2:p.Lys823Asn
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.93A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2517A>C
  hgvsp: ENSP00000412197.2:p.Lys839Asn
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 4.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 9.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 33814
  bin: 2.25e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 3.25e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 2.75e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 1.75e1
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 1.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 8055
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7612
  bin: 9.75e1
  variant carriers: 814
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys858Asn
num of homozygotes: 3
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

17-1372862-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372862
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372862
    reference: chr 17
allele count: 4
allele frequency: 3.72869980237891e-5
allele num: 107276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2468A>T
  hgvsp: ENSP00000459174.1:p.Lys823Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2501A>T
  hgvsp: ENSP00000437685.2:p.Lys834Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2516A>T
  hgvsp: ENSP00000412197.2:p.Lys839Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2468A>T
  hgvsp: ENSP00000354283.2:p.Lys823Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.257A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2573A>T
  hgvsp: ENSP00000352834.5:p.Lys858Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.92A>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8225
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys858Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

17-1372864-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372864
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372864
    reference: chr 17
allele count: 1
allele frequency: 9.31098696461825e-6
allele num: 107400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2499G>C
  hgvsp: ENSP00000437685.2:p.Trp833Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2466G>C
  hgvsp: ENSP00000354283.2:p.Trp822Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.255G>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.90G>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2466G>C
  hgvsp: ENSP00000459174.1:p.Trp822Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2514G>C
  hgvsp: ENSP00000412197.2:p.Trp838Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2571G>C
  hgvsp: ENSP00000352834.5:p.Trp857Cys
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7343
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37636
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6845
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Trp857Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-1372865-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372865
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372865
    reference: chr 17
allele count: 1
allele frequency: 9.306134603930912e-6
allele num: 107456
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2570G>T
  hgvsp: ENSP00000352834.5:p.Trp857Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2465G>T
  hgvsp: ENSP00000354283.2:p.Trp822Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2465G>T
  hgvsp: ENSP00000459174.1:p.Trp822Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2513G>T
  hgvsp: ENSP00000412197.2:p.Trp838Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2498G>T
  hgvsp: ENSP00000437685.2:p.Trp833Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.89G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.254G>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6845
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37713
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Trp857Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-1372867-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372867
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372867
    reference: chr 17
allele count: 1
allele frequency: 9.302325581395349e-6
allele num: 107500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.87G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2568G>T
  hgvsp: ENST00000359786.5:c.2568G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2463G>T
  hgvsp: ENST00000361007.2:c.2463G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2511G>T
  hgvsp: ENST00000438665.2:c.2511G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2496G>T
  hgvsp: ENST00000545534.2:c.2496G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2463G>T
  hgvsp: ENST00000575158.1:c.2463G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.252G>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8304
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6847
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val856Val
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-1372867-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372867
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372867
    reference: chr 17
allele count: 1
allele frequency: 9.302325581395349e-6
allele num: 107500
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2568G>A
  hgvsp: ENST00000359786.5:c.2568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.252G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2463G>A
  hgvsp: ENST00000575158.1:c.2463G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2496G>A
  hgvsp: ENST00000545534.2:c.2496G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2511G>A
  hgvsp: ENST00000438665.2:c.2511G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2463G>A
  hgvsp: ENST00000361007.2:c.2463G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.87G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33538
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8304
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6847
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val856Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

17-1372870-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372870
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372870
    reference: chr 17
allele count: 1
allele frequency: 9.321228165023024e-6
allele num: 107282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2460G>A
  hgvsp: ENSP00000354283.2:p.Met820Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2565G>A
  hgvsp: ENSP00000352834.5:p.Met855Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.84G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2493G>A
  hgvsp: ENSP00000437685.2:p.Met831Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2508G>A
  hgvsp: ENSP00000412197.2:p.Met836Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2460G>A
  hgvsp: ENSP00000459174.1:p.Met820Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.249G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32902
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8588
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36952
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Met855Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-1372872-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372872
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372872
    reference: chr 17
allele count: 2
allele frequency: 1.866995257832045e-5
allele num: 107124
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2506A>G
  hgvsp: ENSP00000412197.2:p.Met836Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2563A>G
  hgvsp: ENSP00000352834.5:p.Met855Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2491A>G
  hgvsp: ENSP00000437685.2:p.Met831Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2458A>G
  hgvsp: ENSP00000354283.2:p.Met820Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2458A>G
  hgvsp: ENSP00000459174.1:p.Met820Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.247A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.82A>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7747
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6844
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8892
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met855Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

17-1372874-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372874
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372874
    reference: chr 17
allele count: 1
allele frequency: 9.340033250518372e-6
allele num: 107066
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.80A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2504A>C
  hgvsp: ENSP00000412197.2:p.Asn835Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2489A>C
  hgvsp: ENSP00000437685.2:p.Asn830Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2561A>C
  hgvsp: ENSP00000352834.5:p.Asn854Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2456A>C
  hgvsp: ENSP00000354283.2:p.Asn819Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2456A>C
  hgvsp: ENSP00000459174.1:p.Asn819Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.245A>C
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn854Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

17-1372879-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372879
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372879
    reference: chr 17
allele count: 1
allele frequency: 9.444832732012316e-6
allele num: 105878
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.240A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2499A>G
  hgvsp: ENSP00000412197.2:p.Ile833Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2556A>G
  hgvsp: ENSP00000352834.5:p.Ile852Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2451A>G
  hgvsp: ENSP00000459174.1:p.Ile817Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.75A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2451A>G
  hgvsp: ENSP00000354283.2:p.Ile817Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2484A>G
  hgvsp: ENSP00000437685.2:p.Ile828Met
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4809
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6842
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile852Met
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

17-1372892-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372892
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372892
    reference: chr 17
allele count: 3
allele frequency: 2.933468924785857e-5
allele num: 102268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2486G>A
  hgvsp: ENSP00000412197.2:p.Arg829Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2438G>A
  hgvsp: ENSP00000354283.2:p.Arg813Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2438G>A
  hgvsp: ENSP00000459174.1:p.Arg813Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.227G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.62G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2471G>A
  hgvsp: ENSP00000437685.2:p.Arg824Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2543G>A
  hgvsp: ENSP00000352834.5:p.Arg848Gln
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25212
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7185
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1928
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28400
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg848Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

17-1372894-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372894
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372894
    reference: chr 17
allele count: 1
allele frequency: 9.802960494069209e-6
allele num: 102010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2484G>A
  hgvsp: ENST00000438665.2:c.2484G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2436G>A
  hgvsp: ENST00000361007.2:c.2436G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2436G>A
  hgvsp: ENST00000575158.1:c.2436G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.225G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2541G>A
  hgvsp: ENST00000359786.5:c.2541G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.60G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2469G>A
  hgvsp: ENST00000545534.2:c.2469G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24781
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1734
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu847Leu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

17-1372899-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372899
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372899
    reference: chr 17
allele count: 2
allele frequency: 1.990842126219391e-5
allele num: 100460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2464C>T
  hgvsp: ENSP00000437685.2:p.Leu822Phe
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.55C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.220C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2536C>T
  hgvsp: ENSP00000352834.5:p.Leu846Phe
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2479C>T
  hgvsp: ENSP00000412197.2:p.Leu827Phe
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2431C>T
  hgvsp: ENSP00000354283.2:p.Leu811Phe
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2431C>T
  hgvsp: ENSP00000459174.1:p.Leu811Phe
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10136
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26336
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu846Phe
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

17-1372901-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372901
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372901
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 99786
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2534A>G
  hgvsp: ENSP00000352834.5:p.Glu845Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2429A>G
  hgvsp: ENSP00000459174.1:p.Glu810Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2477A>G
  hgvsp: ENSP00000412197.2:p.Glu826Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2429A>G
  hgvsp: ENSP00000354283.2:p.Glu810Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.218A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2462A>G
  hgvsp: ENSP00000437685.2:p.Glu821Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.53A>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10348
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6840
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25283
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu845Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-1372917-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372917
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372917
    reference: chr 17
allele count: 1
allele frequency: 1.06136831603303e-5
allele num: 94218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.211-9T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2455-9T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2422-9T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2422-9T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2527-9T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2470-9T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.46-9T>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17669
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15866
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3615
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22952
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4010
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/17-1372920-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372920
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372920
    reference: chr 17
allele count: 1
allele frequency: 1.07670442310177e-5
allele num: 92876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2470-12T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.46-12T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2455-12T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2527-12T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2422-12T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2422-12T>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.211-12T>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10909
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4231
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1850
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12664
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

17-1372930-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372930
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372930
    reference: chr 17
allele count: 1
allele frequency: 1.122914186897837e-5
allele num: 89054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.46-22C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.211-22C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2422-22C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2527-22C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2455-22C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2470-22C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2422-22C>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5338
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7531
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5378
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

17-1372932-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372932
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372932
    reference: chr 17
allele count: 2
allele frequency: 2.257489220488972e-5
allele num: 88594
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.46-24C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2422-24C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.211-24C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2422-24C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2470-24C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2527-24C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2455-24C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22547
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25761
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2065
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5396
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-1372941-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372941
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372941
    reference: chr 17
allele count: 1
allele frequency: 1.203224642040669e-5
allele num: 83110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.211-33G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.46-33G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2422-33G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2422-33G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2470-33G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2455-33G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2527-33G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21837
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15943
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3018
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2035
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3405
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6162
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

17-1372952-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372952
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372952
    reference: chr 17
allele count: 4
allele frequency: 5.208875924575477e-5
allele num: 76792
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2422-44G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2422-44G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2455-44G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2470-44G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.46-44G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2527-44G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.211-44G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7482
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19761
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3785
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3203
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5352
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4570
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6842
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

17-1372956-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1372956
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1372956
    reference: chr 17
allele count: 1
allele frequency: 1.352704055406758e-5
allele num: 73926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2422-48G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2422-48G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2470-48G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2455-48G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.211-48G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.46-48G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2527-48G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19545
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5297
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6062
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6174
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

17-1373431-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373431
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373431
    reference: chr 17
allele count: 1
allele frequency: 1.019451127512947e-5
allele num: 98092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2469+38A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2421+38A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.210+38A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2421+38A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2526+38A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.45+38A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2454+38A>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19511
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9209
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1525
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4468
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2387
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

17-1373439-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373439
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373439
    reference: chr 17
allele count: 1
allele frequency: 1.014075366081207e-5
allele num: 98612
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2421+30A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2454+30A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.210+30A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.45+30A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2421+30A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2469+30A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2526+30A>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10633
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22913
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4297
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3130
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22947
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2923
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-1373443-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373443
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373443
    reference: chr 17
allele count: 1
allele frequency: 1.008491498416668e-5
allele num: 99158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2421+26A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2454+26A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.210+26A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2469+26A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.45+26A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2421+26A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2526+26A>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2480
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3737
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2722
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2186
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

17-1373454-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373454
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373454
    reference: chr 17
allele count: 2
allele frequency: 1.988743710598015e-5
allele num: 100566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2421+15C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2421+15C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2469+15C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.45+15C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2526+15C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.210+15C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2454+15C>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8613
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4626
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

17-1373459-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373459
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373459
    reference: chr 17
allele count: 1
allele frequency: 9.857072449482503e-6
allele num: 101450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2454+10C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.45+10C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.210+10C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2526+10C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2469+10C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2421+10C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2421+10C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28954
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

17-1373461-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373461
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373461
    reference: chr 17
allele count: 2
allele frequency: 1.96313237401598e-5
allele num: 101878
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2454+8G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2526+8G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2469+8G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2421+8G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2421+8G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.210+8G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.45+8G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28022
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8403
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4914
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1929
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 5.75e1
  variant carriers: 0
hgvs: c.2526+8G>A
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

17-1373466-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373466
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373466
    reference: chr 17
allele count: 2
allele frequency: 1.941936110301971e-5
allele num: 102990
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2526+3C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2454+3C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2421+3C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2469+3C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2421+3C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.45+3C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.210+3C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6889
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9852
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1837
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5060
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
hgvs: c.2526+3C>T
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-1373473-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373473
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373473
    reference: chr 17
allele count: 1
allele frequency: 9.638740023904075e-6
allele num: 103748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.41G>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2450G>C
  hgvsp: ENSP00000437685.2:p.Arg817Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2522G>C
  hgvsp: ENSP00000352834.5:p.Arg841Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2465G>C
  hgvsp: ENSP00000412197.2:p.Arg822Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2417G>C
  hgvsp: ENSP00000354283.2:p.Arg806Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.206G>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2417G>C
  hgvsp: ENSP00000459174.1:p.Arg806Pro
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10538
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1881
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7602
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30234
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg841Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

17-1373474-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373474
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373474
    reference: chr 17
allele count: 1
allele frequency: 9.609655782129884e-6
allele num: 104062
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2521C>T
  hgvsp: ENSP00000352834.5:p.Arg841Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2464C>T
  hgvsp: ENSP00000412197.2:p.Arg822Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2416C>T
  hgvsp: ENSP00000459174.1:p.Arg806Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2449C>T
  hgvsp: ENSP00000437685.2:p.Arg817Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2416C>T
  hgvsp: ENSP00000354283.2:p.Arg806Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.205C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.40C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28262
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30301
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1740
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg841Cys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-1373475-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373475
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373475
    reference: chr 17
allele count: 1
allele frequency: 9.595271450229326e-6
allele num: 104218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2463G>C
  hgvsp: ENST00000438665.2:c.2463G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2415G>C
  hgvsp: ENST00000575158.1:c.2415G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2415G>C
  hgvsp: ENST00000361007.2:c.2415G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.39G>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2448G>C
  hgvsp: ENST00000545534.2:c.2448G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2520G>C
  hgvsp: ENST00000359786.5:c.2520G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.204G>C
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1893
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu840Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

17-1373485-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373485
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373485
    reference: chr 17
allele count: 1
allele frequency: 9.506607091928891e-6
allele num: 105190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2405C>T
  hgvsp: ENSP00000354283.2:p.Pro802Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2510C>T
  hgvsp: ENSP00000352834.5:p.Pro837Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.194C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2438C>T
  hgvsp: ENSP00000437685.2:p.Pro813Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.29C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2453C>T
  hgvsp: ENSP00000412197.2:p.Pro818Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2405C>T
  hgvsp: ENSP00000459174.1:p.Pro802Leu
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11381
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26648
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7093
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2004
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro837Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

17-1373487-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373487
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373487
    reference: chr 17
allele count: 1
allele frequency: 9.479751251327165e-6
allele num: 105488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.27C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2403C>T
  hgvsp: ENST00000575158.1:c.2403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2436C>T
  hgvsp: ENST00000545534.2:c.2436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2403C>T
  hgvsp: ENST00000361007.2:c.2403C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2508C>T
  hgvsp: ENST00000359786.5:c.2508C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2451C>T
  hgvsp: ENST00000438665.2:c.2451C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.192C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7249
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2222
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro836Pro
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

17-1373489-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373489
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373489
    reference: chr 17
allele count: 1
allele frequency: 9.473644321497593e-6
allele num: 105556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2449C>T
  hgvsp: ENSP00000412197.2:p.Pro817Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2434C>T
  hgvsp: ENSP00000437685.2:p.Pro812Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2506C>T
  hgvsp: ENSP00000352834.5:p.Pro836Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.190C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2401C>T
  hgvsp: ENSP00000459174.1:p.Pro801Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2401C>T
  hgvsp: ENSP00000354283.2:p.Pro801Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.25C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11433
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 853
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7202
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1185
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro836Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/17-1373490-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373490
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373490
    reference: chr 17
allele count: 5
allele frequency: 4.743562985029315e-5
allele num: 105406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.189G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2505G>T
  hgvsp: ENST00000359786.5:c.2505G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2433G>T
  hgvsp: ENST00000545534.2:c.2433G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2400G>T
  hgvsp: ENST00000575158.1:c.2400G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2448G>T
  hgvsp: ENST00000438665.2:c.2448G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.24G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2400G>T
  hgvsp: ENST00000361007.2:c.2400G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2456
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1887
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1880
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7059
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27247
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1177
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr835Thr
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

17-1373490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373490
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373490
    reference: chr 17
allele count: 4
allele frequency: 3.794850388023452e-5
allele num: 105406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2448G>A
  hgvsp: ENST00000438665.2:c.2448G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2433G>A
  hgvsp: ENST00000545534.2:c.2433G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2505G>A
  hgvsp: ENST00000359786.5:c.2505G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.189G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2400G>A
  hgvsp: ENST00000361007.2:c.2400G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2400G>A
  hgvsp: ENST00000575158.1:c.2400G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.24G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4416
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1674
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1887
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2456
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7059
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2004
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr835Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

17-1373491-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373491
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373491
    reference: chr 17
allele count: 1
allele frequency: 9.46736598943442e-6
allele num: 105626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.188C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2504C>T
  hgvsp: ENSP00000352834.5:p.Thr835Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.23C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2432C>T
  hgvsp: ENSP00000437685.2:p.Thr811Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2447C>T
  hgvsp: ENSP00000412197.2:p.Thr816Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2399C>T
  hgvsp: ENSP00000459174.1:p.Thr800Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2399C>T
  hgvsp: ENSP00000354283.2:p.Thr800Met
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2404
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1764
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5283
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1848
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr835Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-1373491-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373491
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373491
    reference: chr 17
allele count: 1
allele frequency: 9.46736598943442e-6
allele num: 105626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2432C>G
  hgvsp: ENSP00000437685.2:p.Thr811Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2399C>G
  hgvsp: ENSP00000459174.1:p.Thr800Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.188C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2399C>G
  hgvsp: ENSP00000354283.2:p.Thr800Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2504C>G
  hgvsp: ENSP00000352834.5:p.Thr835Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.23C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2447C>G
  hgvsp: ENSP00000412197.2:p.Thr816Arg
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5283
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1954
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1848
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28067
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7145
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr835Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

17-1373491-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373491
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373491
    reference: chr 17
allele count: 1
allele frequency: 9.46736598943442e-6
allele num: 105626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.23C>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2447C>A
  hgvsp: ENSP00000412197.2:p.Thr816Lys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2432C>A
  hgvsp: ENSP00000437685.2:p.Thr811Lys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2399C>A
  hgvsp: ENSP00000459174.1:p.Thr800Lys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2504C>A
  hgvsp: ENSP00000352834.5:p.Thr835Lys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2399C>A
  hgvsp: ENSP00000354283.2:p.Thr800Lys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.188C>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25485
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5283
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1954
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr835Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

17-1373499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373499
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373499
    reference: chr 17
allele count: 2
allele frequency: 1.879063474764177e-5
allele num: 106436
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2439G>A
  hgvsp: ENST00000438665.2:c.2439G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.180G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2424G>A
  hgvsp: ENST00000545534.2:c.2424G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2391G>A
  hgvsp: ENST00000361007.2:c.2391G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2391G>A
  hgvsp: ENST00000575158.1:c.2391G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2496G>A
  hgvsp: ENST00000359786.5:c.2496G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24739
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11526
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1870
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser832Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

17-1373500-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373500
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373500
    reference: chr 17
allele count: 2
allele frequency: 1.877969539334072e-5
allele num: 106498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2438C>T
  hgvsp: ENSP00000412197.2:p.Ser813Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2390C>T
  hgvsp: ENSP00000354283.2:p.Ser797Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.179C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2390C>T
  hgvsp: ENSP00000459174.1:p.Ser797Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2423C>T
  hgvsp: ENSP00000437685.2:p.Ser808Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.14C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2495C>T
  hgvsp: ENSP00000352834.5:p.Ser832Leu
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24533
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2086
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1380
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26356
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser832Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum

17-1373507-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373507
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373507
    reference: chr 17
allele count: 1
allele frequency: 9.343873222328119e-6
allele num: 107022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2383G>C
  hgvsp: ENSP00000354283.2:p.Asp795His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.172G>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2416G>C
  hgvsp: ENSP00000437685.2:p.Asp806His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2383G>C
  hgvsp: ENSP00000459174.1:p.Asp795His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2431G>C
  hgvsp: ENSP00000412197.2:p.Asp811His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.7G>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2488G>C
  hgvsp: ENSP00000352834.5:p.Asp830His
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1683
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23354
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp830His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

17-1373511-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373511
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373511
    reference: chr 17
allele count: 1
allele frequency: 9.335150575978791e-6
allele num: 107122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.168C>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2427C>A
  hgvsp: ENST00000438665.2:c.2427C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2412C>A
  hgvsp: ENST00000545534.2:c.2412C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2379C>A
  hgvsp: ENST00000361007.2:c.2379C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2379C>A
  hgvsp: ENST00000575158.1:c.2379C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2484C>A
  hgvsp: ENST00000359786.5:c.2484C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000574308
  gene symbol: MYO1C
  hgvsc: ENST00000574308.1:n.3C>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11864
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3183
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1778
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2784
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val828Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

17-1373517-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373517
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373517
    reference: chr 17
allele count: 1
allele frequency: 9.354536950420954e-6
allele num: 106900
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2478G>C
  hgvsp: ENSP00000352834.5:p.Gln826His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2406G>C
  hgvsp: ENSP00000437685.2:p.Gln802His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.162G>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2373G>C
  hgvsp: ENSP00000459174.1:p.Gln791His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2421G>C
  hgvsp: ENSP00000412197.2:p.Gln807His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2373G>C
  hgvsp: ENSP00000354283.2:p.Gln791His
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6284
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2897
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6418
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1860
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2794
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 576
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3623
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1832
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln826His
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP

17-1373517-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373517
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373517
    reference: chr 17
allele count: 55
allele frequency: 5.144995322731525e-4
allele num: 106900
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2373G>A
  hgvsp: ENST00000575158.1:c.2373G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2478G>A
  hgvsp: ENST00000359786.5:c.2478G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2406G>A
  hgvsp: ENST00000545534.2:c.2406G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.162G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2373G>A
  hgvsp: ENST00000361007.2:c.2373G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2421G>A
  hgvsp: ENST00000438665.2:c.2421G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22620
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 5207
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6284
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12740
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1962
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1860
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 9.75e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 1832
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1995
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3623
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2794
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3550
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln826Gln
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

17-1373518-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373518
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373518
    reference: chr 17
allele count: 80246
allele frequency: 7.252236782647989e-1
allele num: 110650
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2405A>G
  hgvsp: ENSP00000437685.2:p.Gln802Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2372A>G
  hgvsp: ENSP00000459174.1:p.Gln791Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2420A>G
  hgvsp: ENSP00000412197.2:p.Gln807Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.161A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2372A>G
  hgvsp: ENSP00000354283.2:p.Gln791Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2477A>G
  hgvsp: ENSP00000352834.5:p.Gln826Arg
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 11836
  bin: 2.25e1
  variant carriers: 9881
genotype depth: GenotypeDepth
  all individuals: 7817
  bin: 1.75e1
  variant carriers: 7564
genotype depth: GenotypeDepth
  all individuals: 3198
  bin: 4.25e1
  variant carriers: 3165
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 7.5e0
  variant carriers: 2275
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 3.75e1
  variant carriers: 4905
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 4.75e1
  variant carriers: 1776
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 9.75e1
  variant carriers: 324
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 1.25e1
  variant carriers: 4628
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.5e0
  variant carriers: 375
genotype depth: GenotypeDepth
  all individuals: 10483
  bin: 2.75e1
  variant carriers: 9328
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 369
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 5.25e1
  variant carriers: 997
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 3.25e1
  variant carriers: 7197
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 181
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 5.75e1
  variant carriers: 637
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 263
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 7.5e0
  variant carriers: 274
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 3.25e1
  variant carriers: 1020
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 5.25e1
  variant carriers: 2009
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 1.75e1
  variant carriers: 623
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 4.25e1
  variant carriers: 847
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 2.5e0
  variant carriers: 104
genotype quality: GenotypeQuality
  all individuals: 30369
  bin: 9.75e1
  variant carriers: 30358
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 5.75e1
  variant carriers: 1154
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 2.75e1
  variant carriers: 556
genotype quality: GenotypeQuality
  all individuals: 2485
  bin: 6.75e1
  variant carriers: 2235
genotype quality: GenotypeQuality
  all individuals: 4794
  bin: 6.25e1
  variant carriers: 2280
hgvs: p.Gln826Arg
num of homozygotes: 29171
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

17-1373519-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373519
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373519
    reference: chr 17
allele count: 2
allele frequency: 2.10167924171413e-5
allele num: 95162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2419C>T
  hgvsp: ENSP00000412197.2:p.Gln807Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2371C>T
  hgvsp: ENSP00000354283.2:p.Gln791Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2404C>T
  hgvsp: ENSP00000437685.2:p.Gln802Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2476C>T
  hgvsp: ENSP00000352834.5:p.Gln826Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.160C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2371C>T
  hgvsp: ENSP00000459174.1:p.Gln791Ter
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9029
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16915
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16837
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1048
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln826Ter
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

17-1373530-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373530
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373530
    reference: chr 17
allele count: 1
allele frequency: 1.150642058268514e-5
allele num: 86908
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2465G>C
  hgvsp: ENSP00000352834.5:p.Arg822Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.149G>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2408G>C
  hgvsp: ENSP00000412197.2:p.Arg803Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2393G>C
  hgvsp: ENSP00000437685.2:p.Arg798Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2360G>C
  hgvsp: ENSP00000459174.1:p.Arg787Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2360G>C
  hgvsp: ENSP00000354283.2:p.Arg787Pro
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12228
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20768
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1958
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg822Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-1373530-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373530
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373530
    reference: chr 17
allele count: 1
allele frequency: 1.150642058268514e-5
allele num: 86908
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2408G>A
  hgvsp: ENSP00000412197.2:p.Arg803Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2393G>A
  hgvsp: ENSP00000437685.2:p.Arg798Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2465G>A
  hgvsp: ENSP00000352834.5:p.Arg822Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2360G>A
  hgvsp: ENSP00000354283.2:p.Arg787Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.149G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2360G>A
  hgvsp: ENSP00000459174.1:p.Arg787Gln
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12962
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22965
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1958
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20768
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg822Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

17-1373531-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373531
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373531
    reference: chr 17
allele count: 1
allele frequency: 1.167351512887561e-5
allele num: 85664
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2464C>T
  hgvsp: ENSP00000352834.5:p.Arg822Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2407C>T
  hgvsp: ENSP00000412197.2:p.Arg803Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2359C>T
  hgvsp: ENSP00000459174.1:p.Arg787Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2392C>T
  hgvsp: ENSP00000437685.2:p.Arg798Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2359C>T
  hgvsp: ENSP00000354283.2:p.Arg787Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.148C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23561
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2065
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1962
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2732
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg822Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

17-1373537-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373537
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373537
    reference: chr 17
allele count: 1
allele frequency: 1.224379851605162e-5
allele num: 81674
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2458C>G
  hgvsp: ENSP00000352834.5:p.Leu820Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2353C>G
  hgvsp: ENSP00000459174.1:p.Leu785Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2401C>G
  hgvsp: ENSP00000412197.2:p.Leu801Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2353C>G
  hgvsp: ENSP00000354283.2:p.Leu785Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*186C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2386C>G
  hgvsp: ENSP00000437685.2:p.Leu796Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.142C>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16998
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10233
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26633
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu820Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ

17-1373550-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373550
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373550
    reference: chr 17
allele count: 2
allele frequency: 2.74830978947947e-5
allele num: 72772
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2373T>C
  hgvsp: ENST00000545534.2:c.2373T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2340T>C
  hgvsp: ENST00000361007.2:c.2340T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2340T>C
  hgvsp: ENST00000575158.1:c.2340T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2388T>C
  hgvsp: ENST00000438665.2:c.2388T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2445T>C
  hgvsp: ENST00000359786.5:c.2445T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*173T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.129T>C
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17418
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3690
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31668
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser815Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

17-1373551-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373551
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373551
    reference: chr 17
allele count: 1
allele frequency: 1.377448414556875e-5
allele num: 72598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2387C>G
  hgvsp: ENSP00000412197.2:p.Ser796Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.128C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*172C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2339C>G
  hgvsp: ENSP00000459174.1:p.Ser780Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2444C>G
  hgvsp: ENSP00000352834.5:p.Ser815Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2372C>G
  hgvsp: ENSP00000437685.2:p.Ser791Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2339C>G
  hgvsp: ENSP00000354283.2:p.Ser780Cys
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6279
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6258
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2513
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31868
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10882
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser815Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

17-1373557-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373557
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373557
    reference: chr 17
allele count: 1
allele frequency: 1.47423045170421e-5
allele num: 67832
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2438G>C
  hgvsp: ENSP00000352834.5:p.Arg813Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2333G>C
  hgvsp: ENSP00000459174.1:p.Arg778Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2333G>C
  hgvsp: ENSP00000354283.2:p.Arg778Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2381G>C
  hgvsp: ENSP00000412197.2:p.Arg794Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.122G>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2366G>C
  hgvsp: ENSP00000437685.2:p.Arg789Pro
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*166G>C
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 766
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4836
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg813Pro
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

17-1373557-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373557
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373557
    reference: chr 17
allele count: 1
allele frequency: 1.47423045170421e-5
allele num: 67832
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2333G>A
  hgvsp: ENSP00000354283.2:p.Arg778His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2366G>A
  hgvsp: ENSP00000437685.2:p.Arg789His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*166G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2438G>A
  hgvsp: ENSP00000352834.5:p.Arg813His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.122G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2333G>A
  hgvsp: ENSP00000459174.1:p.Arg778His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2381G>A
  hgvsp: ENSP00000412197.2:p.Arg794His
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18160
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4836
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2605
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg813His
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

17-1373558-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373558
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373558
    reference: chr 17
allele count: 205
allele frequency: 3.056143594024867e-3
allele num: 67078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.121C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2437C>T
  hgvsp: ENSP00000352834.5:p.Arg813Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2365C>T
  hgvsp: ENSP00000437685.2:p.Arg789Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2380C>T
  hgvsp: ENSP00000412197.2:p.Arg794Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*165C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2332C>T
  hgvsp: ENSP00000354283.2:p.Arg778Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2332C>T
  hgvsp: ENSP00000459174.1:p.Arg778Cys
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4660
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 1.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 21298
  bin: 7.5e0
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18114
  bin: 1.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4960
  bin: 2.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4897
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2522
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 1
hgvs: p.Arg813Cys
num of homozygotes: 3
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

17-1373562-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373562
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373562
    reference: chr 17
allele count: 1
allele frequency: 1.544496957340994e-5
allele num: 64746
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2433T>C
  hgvsp: ENST00000359786.5:c.2433T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.117T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2376T>C
  hgvsp: ENST00000438665.2:c.2376T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2328T>C
  hgvsp: ENST00000575158.1:c.2328T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2328T>C
  hgvsp: ENST00000361007.2:c.2328T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*161T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2361T>C
  hgvsp: ENST00000545534.2:c.2361T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5830
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2075
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His811His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

17-1373573-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373573
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373573
    reference: chr 17
allele count: 1
allele frequency: 1.718980988070272e-5
allele num: 58174
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2317T>C
  hgvsp: ENSP00000354283.2:p.Phe773Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2350T>C
  hgvsp: ENSP00000437685.2:p.Phe784Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2422T>C
  hgvsp: ENSP00000352834.5:p.Phe808Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2365T>C
  hgvsp: ENSP00000412197.2:p.Phe789Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.106T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*150T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2317T>C
  hgvsp: ENSP00000459174.1:p.Phe773Leu
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3298
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22121
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9168
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1912
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1285
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe808Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

17-1373580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373580
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373580
    reference: chr 17
allele count: 5
allele frequency: 9.560960685329662e-5
allele num: 52296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.99C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2358C>T
  hgvsp: ENST00000438665.2:c.2358C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2343C>T
  hgvsp: ENST00000545534.2:c.2343C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*143C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2415C>T
  hgvsp: ENST00000359786.5:c.2415C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2310C>T
  hgvsp: ENST00000575158.1:c.2310C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2310C>T
  hgvsp: ENST00000361007.2:c.2310C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16891
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21753
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2499
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12255
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3961
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1806
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 9.75e1
  variant carriers: 6
hgvs: p.Asn805Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

17-1373581-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373581
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373581
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 51956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2342A>G
  hgvsp: ENSP00000437685.2:p.Asn781Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2309A>G
  hgvsp: ENSP00000354283.2:p.Asn770Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2309A>G
  hgvsp: ENSP00000459174.1:p.Asn770Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2414A>G
  hgvsp: ENSP00000352834.5:p.Asn805Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.98A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*142A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2357A>G
  hgvsp: ENSP00000412197.2:p.Asn786Ser
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21739
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11801
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2527
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1854
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn805Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

17-1373585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373585
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373585
    reference: chr 17
allele count: 2
allele frequency: 4.423408678727828e-5
allele num: 45214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2305G>A
  hgvsp: ENSP00000354283.2:p.Glu769Lys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2305G>A
  hgvsp: ENSP00000459174.1:p.Glu769Lys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.94G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2338G>A
  hgvsp: ENSP00000437685.2:p.Glu780Lys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2410G>A
  hgvsp: ENSP00000352834.5:p.Glu804Lys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*138G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2353G>A
  hgvsp: ENSP00000412197.2:p.Glu785Lys
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14565
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14640
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2938
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3045
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24672
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15985
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu804Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

17-1373586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373586
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373586
    reference: chr 17
allele count: 96
allele frequency: 2.317832826307402e-3
allele num: 41418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*137C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2304C>T
  hgvsp: ENST00000361007.2:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.93C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2409C>T
  hgvsp: ENST00000359786.5:c.2409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2304C>T
  hgvsp: ENST00000575158.1:c.2304C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2337C>T
  hgvsp: ENST00000545534.2:c.2337C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2352C>T
  hgvsp: ENST00000438665.2:c.2352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21804
  bin: 7.5e0
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15624
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13055
  bin: 1.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 1.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 8.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22299
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2226
  bin: 2.75e1
  variant carriers: 1
hgvs: p.Pro803Pro
num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

17-1373586-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373586
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373586
    reference: chr 17
allele count: 3
allele frequency: 7.243227582210633e-5
allele num: 41418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2304C>G
  hgvsp: ENST00000575158.1:c.2304C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*137C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2352C>G
  hgvsp: ENST00000438665.2:c.2352C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2337C>G
  hgvsp: ENST00000545534.2:c.2337C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2304C>G
  hgvsp: ENST00000361007.2:c.2304C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.93C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2409C>G
  hgvsp: ENST00000359786.5:c.2409C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21804
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13055
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15624
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22299
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3611
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3427
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro803Pro
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

17-1373588-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373588
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373588
    reference: chr 17
allele count: 1
allele frequency: 2.414992272024729e-5
allele num: 41408
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2407C>T
  hgvsp: ENSP00000352834.5:p.Pro803Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2302C>T
  hgvsp: ENSP00000459174.1:p.Pro768Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2335C>T
  hgvsp: ENSP00000437685.2:p.Pro779Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*135C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.91C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2350C>T
  hgvsp: ENSP00000412197.2:p.Pro784Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2302C>T
  hgvsp: ENSP00000354283.2:p.Pro768Ser
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12876
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15813
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17459
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23039
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1846
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro803Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

17-1373590-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373590
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373590
    reference: chr 17
allele count: 1
allele frequency: 2.435460301997077e-5
allele num: 41060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*133G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2405G>A
  hgvsp: ENSP00000352834.5:p.Cys802Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2300G>A
  hgvsp: ENSP00000459174.1:p.Cys767Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2333G>A
  hgvsp: ENSP00000437685.2:p.Cys778Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2300G>A
  hgvsp: ENSP00000354283.2:p.Cys767Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.89G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2348G>A
  hgvsp: ENSP00000412197.2:p.Cys783Tyr
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12743
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2628
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2176
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Cys802Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/17-1373593-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373593
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373593
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 38262
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2402G>T
  hgvsp: ENSP00000352834.5:p.Arg801Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2330G>T
  hgvsp: ENSP00000437685.2:p.Arg777Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.86G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2297G>T
  hgvsp: ENSP00000459174.1:p.Arg766Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2297G>T
  hgvsp: ENSP00000354283.2:p.Arg766Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*130G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2345G>T
  hgvsp: ENSP00000412197.2:p.Arg782Leu
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22235
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2809
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18325
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg801Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

17-1373593-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373593
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373593
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 38262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2297G>A
  hgvsp: ENSP00000459174.1:p.Arg766His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2330G>A
  hgvsp: ENSP00000437685.2:p.Arg777His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2402G>A
  hgvsp: ENSP00000352834.5:p.Arg801His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2297G>A
  hgvsp: ENSP00000354283.2:p.Arg766His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.86G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2345G>A
  hgvsp: ENSP00000412197.2:p.Arg782His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*130G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22235
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3944
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21523
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18325
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg801His
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

17-1373594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373594
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373594
    reference: chr 17
allele count: 8
allele frequency: 2.15610176800345e-4
allele num: 37104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2296C>T
  hgvsp: ENSP00000459174.1:p.Arg766Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2329C>T
  hgvsp: ENSP00000437685.2:p.Arg777Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2401C>T
  hgvsp: ENSP00000352834.5:p.Arg801Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2296C>T
  hgvsp: ENSP00000354283.2:p.Arg766Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.85C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2344C>T
  hgvsp: ENSP00000412197.2:p.Arg782Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*129C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11360
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22461
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16854
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20798
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1600
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg801Cys
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

17-1373596-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373596
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373596
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 35620
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2294C>G
  hgvsp: ENSP00000459174.1:p.Pro765Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2294C>G
  hgvsp: ENSP00000354283.2:p.Pro765Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2342C>G
  hgvsp: ENSP00000412197.2:p.Pro781Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*127C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2327C>G
  hgvsp: ENSP00000437685.2:p.Pro776Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2399C>G
  hgvsp: ENSP00000352834.5:p.Pro800Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.83C>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22940
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19070
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5003
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro800Arg
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

17-1373597-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1373597
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1373597
    reference: chr 17
allele count: 1
allele frequency: 2.814047726249437e-5
allele num: 35536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459558
  ensembl transcript: ENST00000575011
  gene symbol: MYO1C
  hgvsc: ENST00000575011.1:c.*126C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.2293C>T
  hgvsp: ENSP00000459174.1:p.Pro765Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.2293C>T
  hgvsp: ENSP00000354283.2:p.Pro765Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000197879
  ensembl transcript: ENST00000572615
  gene symbol: MYO1C
  hgvsc: ENST00000572615.1:n.82C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.2398C>T
  hgvsp: ENSP00000352834.5:p.Pro800Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.2341C>T
  hgvsp: ENSP00000412197.2:p.Pro781Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.2326C>T
  hgvsp: ENSP00000437685.2:p.Pro776Ser
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10367
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro800Ser
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 566
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36252
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6866
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.702011777921503e-5
allele num: 58754
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8914
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7846
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5078
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

VQSLOD
type: SiteQuality
SIO_000300: 8.87e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.236e1

DP
type: SiteQuality
SIO_000300: 1.635276e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-1

GenotypeQuality
all individuals: 36571
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.138777841233581e-5
allele num: 14008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5106
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8942
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.050000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

DP
type: SiteQuality
SIO_000300: 1.638713e6

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 5.125e0

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

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

GenotypeQuality
all individuals: 2300
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 66
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 671
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 8.75e1
variant carriers: 11

GenotypeQuality
all individuals: 37290
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 332
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 606
bin: 7.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7962
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.896103896103896e-3
allele num: 770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 94
allele frequency: 1.773584905660378e-2
allele num: 5300
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.324210990951225e-3
allele num: 9062
num of homozygotes: 0

Latino
type: Population
allele count: 34
allele frequency: 3.295212250436131e-3
allele num: 10318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 662
allele frequency: 1.107393777183004e-2
allele num: 59780
num of homozygotes: 2

South Asian
type: Population
allele count: 33
allele frequency: 2.328206575419783e-3
allele num: 14174
num of homozygotes: 1

VQSLOD
type: SiteQuality
SIO_000300: 4.71e0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 1.662905e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 1.312e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

GenotypeQuality
all individuals: 201
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6848
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 247
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37428
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.701514542286557e-5
allele num: 59688
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.076e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.87e-1

QD
type: SiteQuality
SIO_000300: 1.096e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.89e-1

FS
type: SiteQuality
SIO_000300: 9.747e0

DP
type: SiteQuality
SIO_000300: 1.651465e6

VQSLOD
type: SiteQuality
SIO_000300: -1.057e-1

GenotypeQuality
all individuals: 219
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8179
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.674144512154289e-5
allele num: 59732
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14208
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.62e-1

FS
type: SiteQuality
SIO_000300: 1.463e0

MQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

DP
type: SiteQuality
SIO_000300: 1.654178e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.41e-1

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.59e-1

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8183
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9072
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.672912205567452e-5
allele num: 59776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.108e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.109e0

FS
type: SiteQuality
SIO_000300: 1.103e0

QD
type: SiteQuality
SIO_000300: 1.736e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.55e-1

DP
type: SiteQuality
SIO_000300: 1.654608e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.931e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

GenotypeQuality
all individuals: 207
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37627
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 173
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9070
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.672240802675585e-5
allele num: 59800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14216
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.094e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.811e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

DP
type: SiteQuality
SIO_000300: 1.653969e6

QD
type: SiteQuality
SIO_000300: 1.724e1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37627
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.25e-4
allele num: 8000
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9070
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.724e1

VQSLOD
type: SiteQuality
SIO_000300: -3.811e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

FS
type: SiteQuality
SIO_000300: 1.094e0

DP
type: SiteQuality
SIO_000300: 1.653969e6

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-1

GenotypeQuality
all individuals: 543
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6843
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 747
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7964
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.671179883945841e-5
allele num: 10340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9052
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5314
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59628
num of homozygotes: 0

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

QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.021e0

DP
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SIO_000300: 1.651236e6

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -7.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.19e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.359989248034406e-5
allele num: 59524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5312
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9052
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7944
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.385e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.939e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

DP
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SIO_000300: 1.646784e6

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.202e1

FS
type: SiteQuality
SIO_000300: 1.2359e1

MQRankSum
type: SiteQuality
SIO_000300: -9.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.680559290131756e-5
allele num: 59504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9032
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7948
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.78e-1

DP
type: SiteQuality
SIO_000300: 1.645091e6

MQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.143e-1

FS
type: SiteQuality
SIO_000300: 2.552e0

QD
type: SiteQuality
SIO_000300: 6.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.95e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
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allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7842
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.115573404730031e-4
allele num: 8964
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5210
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.311e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.226e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.75e-1

DP
type: SiteQuality
SIO_000300: 1.623765e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 286
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.303534910896874e-5
allele num: 13692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5014
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.51493848857645e-5
allele num: 56900
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.956e1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

QD
type: SiteQuality
SIO_000300: 5.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

FS
type: SiteQuality
SIO_000300: 9.888e0

DP
type: SiteQuality
SIO_000300: 1.564303e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1844
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.316359379572725e-5
allele num: 13668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56748
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.923e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.698e0

FS
type: SiteQuality
SIO_000300: 7.471e0

MQRankSum
type: SiteQuality
SIO_000300: -1.83e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

DP
type: SiteQuality
SIO_000300: 1.556049e6

QD
type: SiteQuality
SIO_000300: 1.141e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55904
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4918
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.171234481143125e-4
allele num: 8538
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 7.380073800738008e-5
allele num: 13550
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.061e0

VQSLOD
type: SiteQuality
SIO_000300: -1.414e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.522736e6

QD
type: SiteQuality
SIO_000300: 1.326e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55536
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4892
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9342
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.65579543714592e-5
allele num: 13062
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52450
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8008
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.93655834850304e-5
allele num: 51638
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 1.349702e6

QD
type: SiteQuality
SIO_000300: 1.546e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.026e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

GenotypeQuality
all individuals: 154
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.020120399175791e-5
allele num: 49502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7708
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.761e0

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.94e-1

DP
type: SiteQuality
SIO_000300: 1.278178e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.331e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 1.712e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

GenotypeQuality
all individuals: 271
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6839
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variant carriers: 2

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.057288919543961e-5
allele num: 49294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7862
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12558
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.2e-2

QD
type: SiteQuality
SIO_000300: 1.228e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

DP
type: SiteQuality
SIO_000300: 1.271856e6

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.05e-1

FS
type: SiteQuality
SIO_000300: 1.219e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.289124668435013e-5
allele num: 12064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7084
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46340
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.076e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

DP
type: SiteQuality
SIO_000300: 1.222198e6

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6806
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.345794392523364e-5
allele num: 42800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11584
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.932e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.073e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

DP
type: SiteQuality
SIO_000300: 1.189527e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.17e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.425889088350881e-5
allele num: 41222
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5828
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4676
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3674
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 3.465e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.34e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 4.26e0

DP
type: SiteQuality
SIO_000300: 1.184033e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4574
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.887308922858158e-5
allele num: 11252
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.77e0

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.116248e6

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.0e-1

QD
type: SiteQuality
SIO_000300: 8.26e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56150
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4618
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8000
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South Asian
type: Population
allele count: 1
allele frequency: 8.788890841975742e-5
allele num: 11378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.475e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.57e1

DP
type: SiteQuality
SIO_000300: 1.154841e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.084e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7566
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.772483959020171e-5
allele num: 56418
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

MQ
type: SiteQuality
SIO_000300: 5.883e1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.178484e6

FS
type: SiteQuality
SIO_000300: 3.764e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.53e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4672
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10460
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.606882168925965e-4
allele num: 7672
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56992
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12016
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MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.5315e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.227319e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1735
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.498480243161094e-5
allele num: 10528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4716
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12274
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.122e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.246284e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.545e0

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.256e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.256e0

FS
type: SiteQuality
SIO_000300: 5.332e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

QD
type: SiteQuality
SIO_000300: 5.13e0

GenotypeQuality
all individuals: 2166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1908
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.46790380609733e-5
allele num: 10562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.737015806843842e-5
allele num: 57570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8134
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7772
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.255086e6

FS
type: SiteQuality
SIO_000300: 1.2227e1

VQSLOD
type: SiteQuality
SIO_000300: -1.727e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.266e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.54000508001016e-4
allele num: 7874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57952
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12862
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.274725e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

QD
type: SiteQuality
SIO_000300: 1.376e1

FS
type: SiteQuality
SIO_000300: 3.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.312e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

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: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1181
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7934
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.347541596560104e-5
allele num: 10698
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4812
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
SIO_000300: 1.288601e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-2

QD
type: SiteQuality
SIO_000300: 9.52e0

GenotypeQuality
all individuals: 1851
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 665
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variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58326
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.474958887726118e-5
allele num: 13378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7948
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

QD
type: SiteQuality
SIO_000300: 1.029e1

VQSLOD
type: SiteQuality
SIO_000300: 4.49e-1

FS
type: SiteQuality
SIO_000300: 2.234e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

DP
type: SiteQuality
SIO_000300: 1.290737e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

GenotypeQuality
all individuals: 1047
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 30499
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variant carriers: 0

GenotypeQuality
all individuals: 1936
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.712974065572647e-5
allele num: 58378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8178
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.292647e6

VQSLOD
type: SiteQuality
SIO_000300: -1.969e-1

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.317e0

MQRankSum
type: SiteQuality
SIO_000300: -4.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.704797299601078e-5
allele num: 58658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10738
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-2

DP
type: SiteQuality
SIO_000300: 1.300566e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.488e0

QD
type: SiteQuality
SIO_000300: 1.036e1

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.511e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.67e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10732
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.068136839129205e-5
allele num: 14148
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

FS
type: SiteQuality
SIO_000300: 3.25e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 7.02e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

DP
type: SiteQuality
SIO_000300: 1.30182e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8132
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Other
type: Population
allele count: 0
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num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.040270346381301e-5
allele num: 14204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58782
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.300651e6

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.869e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.258e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e-1

FS
type: SiteQuality
SIO_000300: 4.151e0

MQRankSum
type: SiteQuality
SIO_000300: 9.85e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.470000000000001e0

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

GenotypeQuality
all individuals: 1059
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.814077884910225e-5
allele num: 58702
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.037297677691766e-5
allele num: 14210
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4806
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.298904e6

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.425e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.887e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.752e0

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

QD
type: SiteQuality
SIO_000300: 8.16e0

GenotypeQuality
all individuals: 1948
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 322
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 865
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5222
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1880
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8142
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.703519471227556e-5
allele num: 58702
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.699136868064119e-4
allele num: 8110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4806
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

MQ
type: SiteQuality
SIO_000300: 5.887e1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e-1

DP
type: SiteQuality
SIO_000300: 1.298904e6

FS
type: SiteQuality
SIO_000300: 3.425e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.752e0

QD
type: SiteQuality
SIO_000300: 8.16e0

GenotypeQuality
all individuals: 1641
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 537
bin: 9.25e1
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GenotypeQuality
all individuals: 1954
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 28067
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58786
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4800
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.229105211406096e-4
allele num: 8136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.022e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.01e-1

QD
type: SiteQuality
SIO_000300: 8.08e0

DP
type: SiteQuality
SIO_000300: 1.302402e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.33e-1

GenotypeQuality
all individuals: 2404
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2014
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variant carriers: 0

GenotypeQuality
all individuals: 484
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variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
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variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1764
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8136
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.337068160597572e-5
allele num: 10710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58786
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.33e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

QD
type: SiteQuality
SIO_000300: 8.08e0

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.022e-1

DP
type: SiteQuality
SIO_000300: 1.302402e6

GenotypeQuality
all individuals: 7145
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1764
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1848
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2404
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28067
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4800
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.701085292416562e-5
allele num: 58786
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.022e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.01e-1

QD
type: SiteQuality
SIO_000300: 8.08e0

DP
type: SiteQuality
SIO_000300: 1.302402e6

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.33e-1

GenotypeQuality
all individuals: 1555
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2075
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5429
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26973
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variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1971
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variant carriers: 2

GenotypeQuality
all individuals: 499
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variant carriers: 0

GenotypeQuality
all individuals: 550
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variant carriers: 0

GenotypeQuality
all individuals: 6935
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.333582228859437e-5
allele num: 10714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.693709562684191e-5
allele num: 59042
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14780
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.304292e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

QD
type: SiteQuality
SIO_000300: 1.04e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.445e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 4.389e0

VQSLOD
type: SiteQuality
SIO_000300: 9.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.094e0

GenotypeQuality
all individuals: 318
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
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variant carriers: 0

GenotypeQuality
all individuals: 6975
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5438
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1092
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1891
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10694
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.34661998384056e-4
allele num: 14852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8272
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.82e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

FS
type: SiteQuality
SIO_000300: 1.746e0

QD
type: SiteQuality
SIO_000300: 1.209e1

DP
type: SiteQuality
SIO_000300: 1.304789e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.09e0

GenotypeQuality
all individuals: 6693
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2798
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5232
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variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 429
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variant carriers: 0

GenotypeQuality
all individuals: 2756
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10680
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.68713726548792e-5
allele num: 59272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15092
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8082
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4806
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

FS
type: SiteQuality
SIO_000300: 5.825e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -6.569e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.822e1

DP
type: SiteQuality
SIO_000300: 1.308099e6

GenotypeQuality
all individuals: 1413
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2890
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1313
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22255
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.686056314280897e-5
allele num: 59310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15164
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4810
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

QD
type: SiteQuality
SIO_000300: 8.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.826e0

FS
type: SiteQuality
SIO_000300: 4.374e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e0

DP
type: SiteQuality
SIO_000300: 1.311847e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

GenotypeQuality
all individuals: 5112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
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variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59158
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.559097468188377e-5
allele num: 15246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7968
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.521e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

FS
type: SiteQuality
SIO_000300: 1.243e0

QD
type: SiteQuality
SIO_000300: 1.401e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

DP
type: SiteQuality
SIO_000300: 1.320901e6

GenotypeQuality
all individuals: 5112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2897
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6418
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
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variant carriers: 0

GenotypeQuality
all individuals: 576
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 18964
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1331
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10602
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4774
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.18962645729241e-4
allele num: 8406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 9.128097636836945e-4
allele num: 59158
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.243e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.401e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.521e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

DP
type: SiteQuality
SIO_000300: 1.320901e6

GenotypeQuality
all individuals: 1855
bin: 9.25e1
variant carriers: 1852

GenotypeQuality
all individuals: 369
bin: 1.25e1
variant carriers: 316

GenotypeQuality
all individuals: 1338
bin: 7.25e1
variant carriers: 1271

GenotypeQuality
all individuals: 2122
bin: 8.25e1
variant carriers: 2104

GenotypeQuality
all individuals: 1467
bin: 3.75e1
variant carriers: 1352

GenotypeQuality
all individuals: 2223
bin: 2.25e1
variant carriers: 823

GenotypeQuality
all individuals: 1120
bin: 8.75e1
variant carriers: 1116

GenotypeQuality
all individuals: 2251
bin: 7.75e1
variant carriers: 2195

GenotypeQuality
all individuals: 1760
bin: 4.75e1
variant carriers: 1670

European (Finnish)
type: Population
allele count: 3553
allele frequency: 6.94759483770043e-1
allele num: 5114
num of homozygotes: 1212

Latino
type: Population
allele count: 7511
allele frequency: 7.028822758749766e-1
allele num: 10686
num of homozygotes: 2598

African
type: Population
allele count: 8174
allele frequency: 8.87320885801129e-1
allele num: 9212
num of homozygotes: 3602

Other
type: Population
allele count: 589
allele frequency: 7.436868686868687e-1
allele num: 792
num of homozygotes: 213

South Asian
type: Population
allele count: 12078
allele frequency: 7.557251908396947e-1
allele num: 15982
num of homozygotes: 4533

East Asian
type: Population
allele count: 3450
allele frequency: 4.329819277108434e-1
allele num: 7968
num of homozygotes: 720

European (Non-Finnish)
type: Population
allele count: 44891
allele frequency: 7.371748554913294e-1
allele num: 60896
num of homozygotes: 16293

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.34e0

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.79e-2

DP
type: SiteQuality
SIO_000300: 1.618663e6

QD
type: SiteQuality
SIO_000300: 2.381e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.103e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1155
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3999
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26244
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.311647429171039e-4
allele num: 7624
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.119464616260858e-5
allele num: 14046
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52710
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3962
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.211093e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

FS
type: SiteQuality
SIO_000300: 6.473e0

QD
type: SiteQuality
SIO_000300: 8.94e0

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.981e0

GenotypeQuality
all individuals: 22965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2881
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1921
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variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7004
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.08420175072947e-5
allele num: 47980
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3550
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

FS
type: SiteQuality
SIO_000300: 1.585e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.085396e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.4e-1

QD
type: SiteQuality
SIO_000300: 7.28e0

VQSLOD
type: SiteQuality
SIO_000300: -2.741e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

GenotypeQuality
all individuals: 2881
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1921
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1193
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6656
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13426
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.427755568246716e-4
allele num: 7004
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47980
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.585e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.4e-1

DP
type: SiteQuality
SIO_000300: 1.085396e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.741e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

QD
type: SiteQuality
SIO_000300: 7.28e0

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 516
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1959
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
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variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 271
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variant carriers: 0

GenotypeQuality
all individuals: 19935
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6940
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.116312537035469e-5
allele num: 47252
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.070803e6

MQRankSum
type: SiteQuality
SIO_000300: 7.37e-1

QD
type: SiteQuality
SIO_000300: 9.390000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.52e-1

FS
type: SiteQuality
SIO_000300: 3.789e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.165e0

VQSLOD
type: SiteQuality
SIO_000300: -2.027e-1

GenotypeQuality
all individuals: 1209
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2099
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variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2410
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17032
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variant carriers: 0

GenotypeQuality
all individuals: 408
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variant carriers: 0

GenotypeQuality
all individuals: 732
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variant carriers: 0

GenotypeQuality
all individuals: 266
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variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.716049382716049e-5
allele num: 12960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7022
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6688
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.683e-1

QD
type: SiteQuality
SIO_000300: 6.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.505e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.19e-1

DP
type: SiteQuality
SIO_000300: 1.00351e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

GenotypeQuality
all individuals: 196
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2525
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
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variant carriers: 0

GenotypeQuality
all individuals: 10581
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
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variant carriers: 0

GenotypeQuality
all individuals: 418
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variant carriers: 0

GenotypeQuality
all individuals: 1838
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variant carriers: 0

GenotypeQuality
all individuals: 631
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variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5476
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.327787021630616e-4
allele num: 6010
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39632
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12198
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.57e0

QD
type: SiteQuality
SIO_000300: 9.17e0

MQ
type: SiteQuality
SIO_000300: 5.871e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

FS
type: SiteQuality
SIO_000300: 4.228e0

DP
type: SiteQuality
SIO_000300: 8.73651e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.835e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.599e0

GenotypeQuality
all individuals: 3697
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 554
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variant carriers: 0

GenotypeQuality
all individuals: 1167
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variant carriers: 0

GenotypeQuality
all individuals: 2281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
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GenotypeQuality
all individuals: 839
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variant carriers: 1

GenotypeQuality
all individuals: 417
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variant carriers: 0

GenotypeQuality
all individuals: 197
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variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.531132935101752e-5
allele num: 39508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5994
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6084
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2814
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.435e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.692e0

MQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.899e0

QD
type: SiteQuality
SIO_000300: 4.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.09e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.762e0

DP
type: SiteQuality
SIO_000300: 8.72982e5

GenotypeQuality
all individuals: 424
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
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variant carriers: 0

GenotypeQuality
all individuals: 562
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GenotypeQuality
all individuals: 2605
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32693
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variant carriers: 0

GenotypeQuality
all individuals: 414
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GenotypeQuality
all individuals: 194
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GenotypeQuality
all individuals: 8261
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variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.721977244270238e-5
allele num: 36738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5670
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.21e-2

QD
type: SiteQuality
SIO_000300: 1.109e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

DP
type: SiteQuality
SIO_000300: 8.21864e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

FS
type: SiteQuality
SIO_000300: 2.463e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1057
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1585
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variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
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variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5466
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.721977244270238e-5
allele num: 36738
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2624
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

QD
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.463e0

MQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.21e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 9
allele frequency: 2.479338842975207e-4
allele num: 36300
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 8.507742045261188e-5
allele num: 11754
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2580
num of homozygotes: 0

Latino
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allele count: 13
allele frequency: 2.432634730538922e-3
allele num: 5344
num of homozygotes: 0

African
type: Population
allele count: 181
allele frequency: 3.230988932524099e-2
allele num: 5602
num of homozygotes: 3

Other
type: Population
allele count: 1
allele frequency: 2.049180327868853e-3
allele num: 488
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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MQRankSum
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BaseQRankSum
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SIO_000300: -1.133e0

ClippingRankSum
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.14e-2

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.858286171611502e-5
allele num: 34986
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2440
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African
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allele frequency: 0.0e0
allele num: 5342
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South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5152
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.44e-2

MQ
type: SiteQuality
SIO_000300: 5.838e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 7.84832e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.89e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.202049311559398e-5
allele num: 31230
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2082
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4276
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4804
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10954
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.16003e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.99e-2

FS
type: SiteQuality
SIO_000300: 2.537e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
SIO_000300: 8.210000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -4.526e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 373
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variant carriers: 2

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

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

African
type: Population
allele count: 1
allele frequency: 2.303086135421465e-4
allele num: 4342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.44102601051949e-4
allele num: 27758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1748
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3728
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10546
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.177e1

MQRankSum
type: SiteQuality
SIO_000300: 6.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.658e0

FS
type: SiteQuality
SIO_000300: 2.049e0

DP
type: SiteQuality
SIO_000300: 6.70032e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.62e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3782
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3674
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27552
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-2

QD
type: SiteQuality
SIO_000300: 8.470000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

DP
type: SiteQuality
SIO_000300: 6.63613e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.011e0

FS
type: SiteQuality
SIO_000300: 3.169e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.53e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23630
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 7.473841554559044e-4
allele num: 1338
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.978048293753742e-5
allele num: 10022
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MQ
type: SiteQuality
SIO_000300: 5.896e1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.791e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.231e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 100

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21352
num of homozygotes: 0

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

East Asian
type: Population
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allele num: 2920
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South Asian
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African
type: Population
allele count: 95
allele frequency: 2.692743764172336e-2
allele num: 3528
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2446
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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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: 2930
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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
type: Population
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allele frequency: 2.873563218390805e-4
allele num: 3480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1136
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 302
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21328
num of homozygotes: 0

South Asian
type: Population
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2480
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.844e1

MQRankSum
type: SiteQuality
SIO_000300: -5.09e-1

FS
type: SiteQuality
SIO_000300: 5.909e0

VQSLOD
type: SiteQuality
SIO_000300: -8.083e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.43e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.157e0

DP
type: SiteQuality
SIO_000300: 5.94228e5

QD
type: SiteQuality
SIO_000300: 1.776e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
all individuals: 23399
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2622
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3554
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 348
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2908
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.030078285949732e-4
allele num: 9708
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3450
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.43e-1

QD
type: SiteQuality
SIO_000300: 4.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.856e0

VQSLOD
type: SiteQuality
SIO_000300: -1.691e0

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.46e-2

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 1.808e0

DP
type: SiteQuality
SIO_000300: 5.91703e5

GenotypeQuality
all individuals: 3944
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21523
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 974
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19492
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.80168e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.403e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.24e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2044
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2809
bin: 1.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1604
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2402
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 974
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19492
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.95e0

DP
type: SiteQuality
SIO_000300: 5.80168e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
all individuals: 4311
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2635
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19066
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2382
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.324246619103397e-5
allele num: 18782
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 7.923930269413629e-4
allele num: 2524
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 5.348737697903295e-4
allele num: 9348
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.403e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.22e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

QD
type: SiteQuality
SIO_000300: 1.145e1

DP
type: SiteQuality
SIO_000300: 5.69871e5

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.75e-1

GenotypeQuality
all individuals: 674
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20039
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
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variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
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variant carriers: 1

GenotypeQuality
all individuals: 863
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1858
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.86e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

VQSLOD
type: SiteQuality
SIO_000300: -2.198e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 5.54017e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

QD
type: SiteQuality
SIO_000300: 1.186e1