http://identifiers.org/exac.variant/17-34871700-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871700
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871700
    reference: chr 17
allele count: 2
allele frequency: 1.675575141167206e-5
allele num: 119362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.547+1G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.547+1G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.547+1G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.547+1G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.547+1G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.145+1G>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2521
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1532
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2191
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 3.75e1
  variant carriers: 0
hgvs: c.547+1G>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

17-34871705-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871705
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871705
    reference: chr 17
allele count: 1
allele frequency: 8.353381448810478e-6
allele num: 119712
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.141T>C
  hgvsp: ENST00000544606.1:c.141T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.543T>C
  hgvsp: ENST00000586007.1:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.543T>C
  hgvsp: ENST00000431794.3:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.543T>C
  hgvsp: ENST00000586908.1:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.543T>C
  hgvsp: ENST00000268852.9:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.543T>C
  hgvsp: ENST00000591794.1:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23471
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2525
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala181Ala
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

17-34871708-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871708
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871708
    reference: chr 17
allele count: 1
allele frequency: 8.34432002136146e-6
allele num: 119842
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.540A>C
  hgvsp: ENSP00000409936.2:p.Glu180Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.540A>C
  hgvsp: ENSP00000468792.1:p.Glu180Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.138A>C
  hgvsp: ENSP00000438365.1:p.Glu46Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.540A>C
  hgvsp: ENSP00000468488.1:p.Glu180Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.540A>C
  hgvsp: ENSP00000268852.8:p.Glu180Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.540A>C
  hgvsp: ENSP00000466786.1:p.Glu180Asp
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23514
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6978
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1535
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2528
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4343
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu180Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

17-34871709-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871709
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871709
    reference: chr 17
allele count: 1
allele frequency: 8.34125752798492e-6
allele num: 119886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.539A>G
  hgvsp: ENSP00000468792.1:p.Glu180Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.539A>G
  hgvsp: ENSP00000468488.1:p.Glu180Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.539A>G
  hgvsp: ENSP00000466786.1:p.Glu180Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.137A>G
  hgvsp: ENSP00000438365.1:p.Glu46Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.539A>G
  hgvsp: ENSP00000409936.2:p.Glu180Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.539A>G
  hgvsp: ENSP00000268852.8:p.Glu180Gly
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39705
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2197
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6977
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Glu180Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP

17-34871713-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871713
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871713
    reference: chr 17
allele count: 2
allele frequency: 1.666555562962469e-5
allele num: 120008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.535A>T
  hgvsp: ENSP00000468488.1:p.Met179Leu
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.535A>T
  hgvsp: ENSP00000466786.1:p.Met179Leu
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.535A>T
  hgvsp: ENSP00000468792.1:p.Met179Leu
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.535A>T
  hgvsp: ENSP00000409936.2:p.Met179Leu
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.133A>T
  hgvsp: ENSP00000438365.1:p.Met45Leu
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.535A>T
  hgvsp: ENSP00000268852.8:p.Met179Leu
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39735
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2190
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2536
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Met179Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

17-34871713-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871713
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871713
    reference: chr 17
allele count: 13
allele frequency: 1.083261115925605e-4
allele num: 120008
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.535A>C
  hgvsp: ENSP00000409936.2:p.Met179Leu
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.535A>C
  hgvsp: ENSP00000468792.1:p.Met179Leu
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.535A>C
  hgvsp: ENSP00000468488.1:p.Met179Leu
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.133A>C
  hgvsp: ENSP00000438365.1:p.Met45Leu
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.535A>C
  hgvsp: ENSP00000268852.8:p.Met179Leu
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.535A>C
  hgvsp: ENSP00000466786.1:p.Met179Leu
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23483
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23497
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4355
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1535
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6980
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2536
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Met179Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

17-34871714-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871714
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871714
    reference: chr 17
allele count: 1
allele frequency: 8.331389342486753e-6
allele num: 120028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.534C>T
  hgvsp: ENST00000268852.9:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.534C>T
  hgvsp: ENST00000586908.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.534C>T
  hgvsp: ENST00000591794.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.534C>T
  hgvsp: ENST00000431794.3:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.132C>T
  hgvsp: ENST00000544606.1:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.534C>T
  hgvsp: ENST00000586007.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val178Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

17-34871717-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871717
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871717
    reference: chr 17
allele count: 2
allele frequency: 1.665168015452759e-5
allele num: 120108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.531T>C
  hgvsp: ENST00000586007.1:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.129T>C
  hgvsp: ENST00000544606.1:c.129T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.531T>C
  hgvsp: ENST00000431794.3:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.531T>C
  hgvsp: ENST00000268852.9:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.531T>C
  hgvsp: ENST00000591794.1:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.531T>C
  hgvsp: ENST00000586908.1:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6993
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2536
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro177Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD

17-34871718-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871718
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871718
    reference: chr 17
allele count: 1
allele frequency: 8.326533331112925e-6
allele num: 120098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.128C>G
  hgvsp: ENSP00000438365.1:p.Pro43Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.530C>G
  hgvsp: ENSP00000468792.1:p.Pro177Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.530C>G
  hgvsp: ENSP00000409936.2:p.Pro177Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.530C>G
  hgvsp: ENSP00000466786.1:p.Pro177Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.530C>G
  hgvsp: ENSP00000468488.1:p.Pro177Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.530C>G
  hgvsp: ENSP00000268852.8:p.Pro177Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.530C>G
  hgvsp: ENST00000585719.1:c.530C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2187
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39893
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2531
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro177Arg
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

17-34871720-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871720
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871720
    reference: chr 17
allele count: 1
allele frequency: 8.323899580475461e-6
allele num: 120136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.528C>T
  hgvsp: ENST00000268852.9:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.528C>T
  hgvsp: ENST00000586908.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.528C>T
  hgvsp: ENST00000585719.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.528C>T
  hgvsp: ENST00000586007.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.126C>T
  hgvsp: ENST00000544606.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.528C>T
  hgvsp: ENST00000591794.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.528C>T
  hgvsp: ENST00000431794.3:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39874
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2537
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4347
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn176Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

17-34871721-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871721
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871721
    reference: chr 17
allele count: 7447
allele frequency: 6.197466753216491e-2
allele num: 120162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.527A>G
  hgvsp: ENSP00000268852.8:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.527A>G
  hgvsp: ENSP00000409936.2:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.527A>G
  hgvsp: ENSP00000465350.1:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.527A>G
  hgvsp: ENSP00000468488.1:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.527A>G
  hgvsp: ENSP00000468792.1:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.527A>G
  hgvsp: ENSP00000466786.1:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.125A>G
  hgvsp: ENSP00000438365.1:p.Asn42Ser
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.25e1
  variant carriers: 403
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.75e1
  variant carriers: 573
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 4.75e1
  variant carriers: 848
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 4.25e1
  variant carriers: 938
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.75e1
  variant carriers: 900
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.75e1
  variant carriers: 397
genotype depth: GenotypeDepth
  all individuals: 21639
  bin: 2.25e1
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.25e1
  variant carriers: 197
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 22478
  bin: 2.75e1
  variant carriers: 458
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 734
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 3.25e1
  variant carriers: 672
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6177
  bin: 6.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 8.25e1
  variant carriers: 19
hgvs: p.Asn176Ser
num of homozygotes: 340
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

17-34871726-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871726
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871726
    reference: chr 17
allele count: 1
allele frequency: 8.320159747067144e-6
allele num: 120190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.522C>T
  hgvsp: ENST00000586908.1:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.522C>T
  hgvsp: ENST00000586007.1:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.522C>T
  hgvsp: ENST00000268852.9:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.120C>T
  hgvsp: ENST00000544606.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.522C>T
  hgvsp: ENST00000431794.3:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.522C>T
  hgvsp: ENST00000591794.1:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.522C>T
  hgvsp: ENST00000585719.1:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25806
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2474
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7138
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn174Asn
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ

17-34871736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871736
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871736
    reference: chr 17
allele count: 1
allele frequency: 8.324592511196577e-6
allele num: 120126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.512G>A
  hgvsp: ENSP00000468792.1:p.Arg171Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.512G>A
  hgvsp: ENSP00000409936.2:p.Arg171Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.110G>A
  hgvsp: ENSP00000438365.1:p.Arg37Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.512G>A
  hgvsp: ENSP00000465350.1:p.Arg171Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.512G>A
  hgvsp: ENSP00000268852.8:p.Arg171Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.512G>A
  hgvsp: ENSP00000466786.1:p.Arg171Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.512G>A
  hgvsp: ENSP00000468488.1:p.Arg171Lys
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7050
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42606
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg171Lys
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

17-34871738-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871738
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871738
    reference: chr 17
allele count: 1
allele frequency: 8.326949338840222e-6
allele num: 120092
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.108G>C
  hgvsp: ENSP00000438365.1:p.Gln36His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.510G>C
  hgvsp: ENSP00000409936.2:p.Gln170His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.510G>C
  hgvsp: ENSP00000468792.1:p.Gln170His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.510G>C
  hgvsp: ENSP00000468488.1:p.Gln170His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.510G>C
  hgvsp: ENSP00000465350.1:p.Gln170His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.510G>C
  hgvsp: ENSP00000268852.8:p.Gln170His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.510G>C
  hgvsp: ENSP00000466786.1:p.Gln170His
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7013
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2472
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln170His
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

17-34871738-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871738
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871738
    reference: chr 17
allele count: 1
allele frequency: 8.326949338840222e-6
allele num: 120092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.510G>A
  hgvsp: ENST00000586007.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.510G>A
  hgvsp: ENST00000585719.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.510G>A
  hgvsp: ENST00000591794.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.510G>A
  hgvsp: ENST00000586908.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.510G>A
  hgvsp: ENST00000268852.9:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.108G>A
  hgvsp: ENST00000544606.1:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.510G>A
  hgvsp: ENST00000431794.3:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln170Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

17-34871740-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871740
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871740
    reference: chr 17
allele count: 2
allele frequency: 1.665278934221482e-5
allele num: 120100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.508C>A
  hgvsp: ENSP00000468488.1:p.Gln170Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.508C>A
  hgvsp: ENSP00000468792.1:p.Gln170Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.106C>A
  hgvsp: ENSP00000438365.1:p.Gln36Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.508C>A
  hgvsp: ENSP00000466786.1:p.Gln170Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.508C>A
  hgvsp: ENSP00000465350.1:p.Gln170Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.508C>A
  hgvsp: ENSP00000268852.8:p.Gln170Lys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.508C>A
  hgvsp: ENSP00000409936.2:p.Gln170Lys
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6218
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42583
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln170Lys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/17-34871743-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871743
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871743
    reference: chr 17
allele count: 1
allele frequency: 8.328058896032513e-6
allele num: 120076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.103G>T
  hgvsp: ENSP00000438365.1:p.Glu35Ter
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.505G>T
  hgvsp: ENSP00000409936.2:p.Glu169Ter
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.505G>T
  hgvsp: ENSP00000468792.1:p.Glu169Ter
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.505G>T
  hgvsp: ENSP00000468488.1:p.Glu169Ter
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.505G>T
  hgvsp: ENSP00000466786.1:p.Glu169Ter
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.505G>T
  hgvsp: ENSP00000465350.1:p.Glu169Ter
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.505G>T
  hgvsp: ENSP00000268852.8:p.Glu169Ter
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu169Ter
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

17-34871750-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871750
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871750
    reference: chr 17
allele count: 1
allele frequency: 8.33625102119075e-6
allele num: 119958
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.498G>C
  hgvsp: ENSP00000268852.8:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.498G>C
  hgvsp: ENSP00000409936.2:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.498G>C
  hgvsp: ENSP00000468488.1:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.498G>C
  hgvsp: ENSP00000466786.1:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.96G>C
  hgvsp: ENSP00000438365.1:p.Glu32Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.498G>C
  hgvsp: ENSP00000465350.1:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.498G>C
  hgvsp: ENSP00000468792.1:p.Glu166Asp
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42508
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu166Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

17-34871756-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871756
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871756
    reference: chr 17
allele count: 1
allele frequency: 8.34599142032082e-6
allele num: 119818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.492T>A
  hgvsp: ENST00000591794.1:c.492T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.90T>A
  hgvsp: ENST00000544606.1:c.90T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.492T>A
  hgvsp: ENST00000586908.1:c.492T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.492T>A
  hgvsp: ENST00000268852.9:c.492T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.492T>A
  hgvsp: ENST00000586007.1:c.492T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.492T>A
  hgvsp: ENST00000585719.1:c.492T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.492T>A
  hgvsp: ENST00000431794.3:c.492T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22718
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2464
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42350
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile164Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

17-34871762-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871762
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871762
    reference: chr 17
allele count: 1
allele frequency: 8.360924383799873e-6
allele num: 119604
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.486C>T
  hgvsp: ENST00000589404.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.486C>T
  hgvsp: ENST00000431794.3:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.486C>T
  hgvsp: ENST00000586007.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.486C>T
  hgvsp: ENST00000591794.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.84C>T
  hgvsp: ENST00000544606.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.486C>T
  hgvsp: ENST00000268852.9:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.486C>T
  hgvsp: ENST00000586908.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.486C>T
  hgvsp: ENST00000585719.1:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22546
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6705
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His162His
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

17-34871763-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871763
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871763
    reference: chr 17
allele count: 1
allele frequency: 8.364281173675934e-6
allele num: 119556
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.485A>C
  hgvsp: ENSP00000268852.8:p.His162Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.485A>C
  hgvsp: ENSP00000468488.1:p.His162Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.485A>C
  hgvsp: ENSP00000466786.1:p.His162Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.485A>C
  hgvsp: ENSP00000409936.2:p.His162Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.83A>C
  hgvsp: ENSP00000438365.1:p.His28Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.485A>C
  hgvsp: ENSP00000467285.1:p.His162Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.485A>C
  hgvsp: ENSP00000465350.1:p.His162Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.485A>C
  hgvsp: ENSP00000468792.1:p.His162Pro
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1066
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His162Pro
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

17-34871775-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871775
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871775
    reference: chr 17
allele count: 2
allele frequency: 1.681916038751345e-5
allele num: 118912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.473C>T
  hgvsp: ENSP00000268852.8:p.Ser158Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.473C>T
  hgvsp: ENSP00000466786.1:p.Ser158Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.473C>T
  hgvsp: ENSP00000465350.1:p.Ser158Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.473C>T
  hgvsp: ENSP00000467285.1:p.Ser158Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.71C>T
  hgvsp: ENSP00000438365.1:p.Ser24Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.473C>T
  hgvsp: ENSP00000468792.1:p.Ser158Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.473C>T
  hgvsp: ENSP00000468488.1:p.Ser158Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.473C>T
  hgvsp: ENSP00000409936.2:p.Ser158Phe
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24555
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40463
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1911
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser158Phe
num of homozygotes: 1
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

17-34871775-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871775
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871775
    reference: chr 17
allele count: 12
allele frequency: 1.009149623250807e-4
allele num: 118912
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.473C>G
  hgvsp: ENSP00000467285.1:p.Ser158Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.473C>G
  hgvsp: ENSP00000468792.1:p.Ser158Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.473C>G
  hgvsp: ENSP00000409936.2:p.Ser158Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.473C>G
  hgvsp: ENSP00000268852.8:p.Ser158Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.71C>G
  hgvsp: ENSP00000438365.1:p.Ser24Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.473C>G
  hgvsp: ENSP00000466786.1:p.Ser158Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.473C>G
  hgvsp: ENSP00000465350.1:p.Ser158Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.473C>G
  hgvsp: ENSP00000468488.1:p.Ser158Cys
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22366
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24555
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1911
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser158Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/17-34871779-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871779
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871779
    reference: chr 17
allele count: 1
allele frequency: 8.426445556735258e-6
allele num: 118674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.469G>T
  hgvsp: ENSP00000468488.1:p.Ala157Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.469G>T
  hgvsp: ENSP00000468792.1:p.Ala157Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.469G>T
  hgvsp: ENSP00000467285.1:p.Ala157Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.469G>T
  hgvsp: ENSP00000466786.1:p.Ala157Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.469G>T
  hgvsp: ENSP00000409936.2:p.Ala157Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.469G>T
  hgvsp: ENSP00000465350.1:p.Ala157Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.67G>T
  hgvsp: ENSP00000438365.1:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.469G>T
  hgvsp: ENSP00000268852.8:p.Ala157Ser
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1936
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6322
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala157Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

17-34871790-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871790
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871790
    reference: chr 17
allele count: 2
allele frequency: 1.694943982101392e-5
allele num: 117998
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.458C>T
  hgvsp: ENSP00000467285.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.458C>T
  hgvsp: ENSP00000465350.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.458C>T
  hgvsp: ENSP00000466786.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.458C>T
  hgvsp: ENSP00000468792.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.458C>T
  hgvsp: ENSP00000268852.8:p.Ala153Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.56C>T
  hgvsp: ENSP00000438365.1:p.Ala19Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.458C>T
  hgvsp: ENSP00000409936.2:p.Ala153Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.458C>T
  hgvsp: ENSP00000468488.1:p.Ala153Val
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5428
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5951
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1674
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39682
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala153Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

17-34871793-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871793
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871793
    reference: chr 17
allele count: 1
allele frequency: 8.490982576503753e-6
allele num: 117772
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.455T>C
  hgvsp: ENSP00000465350.1:p.Val152Ala
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.455T>C
  hgvsp: ENSP00000268852.8:p.Val152Ala
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.455T>C
  hgvsp: ENSP00000409936.2:p.Val152Ala
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.455T>C
  hgvsp: ENSP00000468792.1:p.Val152Ala
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.455T>C
  hgvsp: ENSP00000468488.1:p.Val152Ala
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.455T>C
  hgvsp: ENSP00000466786.1:p.Val152Ala
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.53T>C
  hgvsp: ENSP00000438365.1:p.Val18Ala
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.455T>C
  hgvsp: ENSP00000467285.1:p.Val152Ala
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val152Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-34871794-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871794
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871794
    reference: chr 17
allele count: 1
allele frequency: 8.49314603115286e-6
allele num: 117742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.454G>A
  hgvsp: ENSP00000468488.1:p.Val152Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.454G>A
  hgvsp: ENSP00000465350.1:p.Val152Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.454G>A
  hgvsp: ENSP00000467285.1:p.Val152Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.52G>A
  hgvsp: ENSP00000438365.1:p.Val18Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.454G>A
  hgvsp: ENSP00000466786.1:p.Val152Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.454G>A
  hgvsp: ENSP00000268852.8:p.Val152Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.454G>A
  hgvsp: ENSP00000468792.1:p.Val152Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.454G>A
  hgvsp: ENSP00000409936.2:p.Val152Met
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23312
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40265
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2811
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5818
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val152Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

17-34871795-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871795
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871795
    reference: chr 17
allele count: 1
allele frequency: 8.498631720293032e-6
allele num: 117666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.453G>A
  hgvsp: ENST00000586908.1:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.453G>A
  hgvsp: ENST00000591794.1:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.453G>A
  hgvsp: ENST00000589404.1:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.453G>A
  hgvsp: ENST00000586007.1:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.51G>A
  hgvsp: ENST00000544606.1:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.453G>A
  hgvsp: ENST00000268852.9:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.453G>A
  hgvsp: ENST00000585719.1:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.453G>A
  hgvsp: ENST00000431794.3:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1600
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val151Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

17-34871802-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871802
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871802
    reference: chr 17
allele count: 164
allele frequency: 1.40209288010396e-3
allele num: 116968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.44A>G
  hgvsp: ENSP00000438365.1:p.Tyr15Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.446A>G
  hgvsp: ENSP00000268852.8:p.Tyr149Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.446A>G
  hgvsp: ENSP00000467285.1:p.Tyr149Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.446A>G
  hgvsp: ENSP00000468488.1:p.Tyr149Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.446A>G
  hgvsp: ENSP00000409936.2:p.Tyr149Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.446A>G
  hgvsp: ENSP00000468792.1:p.Tyr149Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.446A>G
  hgvsp: ENSP00000465350.1:p.Tyr149Cys
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.446A>G
  hgvsp: ENSP00000466786.1:p.Tyr149Cys
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22763
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 22682
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 3509
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5474
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr149Cys
num of homozygotes: 1
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

17-34871812-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871812
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871812
    reference: chr 17
allele count: 2
allele frequency: 1.738797795204396e-5
allele num: 115022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.436A>G
  hgvsp: ENSP00000468792.1:p.Met146Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.436A>G
  hgvsp: ENSP00000468488.1:p.Met146Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.436A>G
  hgvsp: ENSP00000268852.8:p.Met146Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.34A>G
  hgvsp: ENSP00000438365.1:p.Met12Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.436A>G
  hgvsp: ENSP00000466786.1:p.Met146Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.436A>G
  hgvsp: ENSP00000465350.1:p.Met146Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.436A>G
  hgvsp: ENSP00000409936.2:p.Met146Val
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.436A>G
  hgvsp: ENSP00000467285.1:p.Met146Val
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21827
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5439
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Met146Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-34871813-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871813
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871813
    reference: chr 17
allele count: 4876
allele frequency: 4.247460757156048e-2
allele num: 114798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.33A>G
  hgvsp: ENST00000544606.1:c.33A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.435A>G
  hgvsp: ENST00000586908.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.435A>G
  hgvsp: ENST00000431794.3:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.435A>G
  hgvsp: ENST00000585719.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.435A>G
  hgvsp: ENST00000589404.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.435A>G
  hgvsp: ENST00000586007.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.435A>G
  hgvsp: ENST00000591794.1:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.435A>G
  hgvsp: ENST00000268852.9:c.435A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 20575
  bin: 2.25e1
  variant carriers: 565
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 1.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.25e1
  variant carriers: 403
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 3.75e1
  variant carriers: 638
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.75e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 1.75e1
  variant carriers: 323
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.75e1
  variant carriers: 253
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 21299
  bin: 2.75e1
  variant carriers: 764
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.25e1
  variant carriers: 196
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.75e1
  variant carriers: 180
genotype depth: GenotypeDepth
  all individuals: 4989
  bin: 3.25e1
  variant carriers: 819
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 4.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4447
  bin: 6.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 36475
  bin: 6.25e1
  variant carriers: 11
hgvs: p.Leu145Leu
num of homozygotes: 160
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

17-34871819-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871819
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871819
    reference: chr 17
allele count: 789
allele frequency: 6.988609187053801e-3
allele num: 112898
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.429C>T
  hgvsp: ENST00000431794.3:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.27C>T
  hgvsp: ENST00000544606.1:c.27C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.429C>T
  hgvsp: ENST00000585719.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.429C>T
  hgvsp: ENST00000591794.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.429C>T
  hgvsp: ENST00000586007.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.429C>T
  hgvsp: ENST00000586908.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.429C>T
  hgvsp: ENST00000589404.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.429C>T
  hgvsp: ENST00000268852.9:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 3.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 3836
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 21117
  bin: 2.75e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 20711
  bin: 2.25e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 1.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 1.75e1
  variant carriers: 85
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 9.75e1
  variant carriers: 732
hgvs: p.Arg143Arg
num of homozygotes: 32
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

17-34871820-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871820
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871820
    reference: chr 17
allele count: 1
allele frequency: 8.892999430848037e-6
allele num: 112448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.428G>C
  hgvsp: ENSP00000466786.1:p.Arg143Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.428G>C
  hgvsp: ENSP00000468792.1:p.Arg143Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.26G>C
  hgvsp: ENSP00000438365.1:p.Arg9Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.428G>C
  hgvsp: ENSP00000268852.8:p.Arg143Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.428G>C
  hgvsp: ENSP00000465350.1:p.Arg143Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.428G>C
  hgvsp: ENSP00000467285.1:p.Arg143Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.428G>C
  hgvsp: ENSP00000409936.2:p.Arg143Pro
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.428G>C
  hgvsp: ENSP00000468488.1:p.Arg143Pro
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1372
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg143Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

17-34871820-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871820
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871820
    reference: chr 17
allele count: 3
allele frequency: 2.667899829254411e-5
allele num: 112448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.428G>A
  hgvsp: ENSP00000467285.1:p.Arg143His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.428G>A
  hgvsp: ENSP00000466786.1:p.Arg143His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.428G>A
  hgvsp: ENSP00000268852.8:p.Arg143His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.428G>A
  hgvsp: ENSP00000465350.1:p.Arg143His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.26G>A
  hgvsp: ENSP00000438365.1:p.Arg9His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.428G>A
  hgvsp: ENSP00000468488.1:p.Arg143His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.428G>A
  hgvsp: ENSP00000409936.2:p.Arg143His
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.428G>A
  hgvsp: ENSP00000468792.1:p.Arg143His
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20667
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4429
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37423
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg143His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

17-34871823-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871823
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871823
    reference: chr 17
allele count: 6
allele frequency: 5.37480292389279e-5
allele num: 111632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.425C>T
  hgvsp: ENSP00000468792.1:p.Ser142Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.425C>T
  hgvsp: ENSP00000467285.1:p.Ser142Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.425C>T
  hgvsp: ENSP00000268852.8:p.Ser142Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.23C>T
  hgvsp: ENSP00000438365.1:p.Ser8Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.425C>T
  hgvsp: ENSP00000465350.1:p.Ser142Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.425C>T
  hgvsp: ENSP00000468488.1:p.Ser142Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.425C>T
  hgvsp: ENSP00000409936.2:p.Ser142Phe
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.425C>T
  hgvsp: ENSP00000466786.1:p.Ser142Phe
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7346
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20170
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9134
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1031
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser142Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

17-34871825-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871825
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871825
    reference: chr 17
allele count: 31
allele frequency: 2.792189076235769e-4
allele num: 111024
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.423G>A
  hgvsp: ENST00000431794.3:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.423G>A
  hgvsp: ENST00000586908.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.423G>A
  hgvsp: ENST00000586007.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.423G>A
  hgvsp: ENST00000591794.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.423G>A
  hgvsp: ENST00000268852.9:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.21G>A
  hgvsp: ENST00000544606.1:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.423G>A
  hgvsp: ENST00000585719.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.423G>A
  hgvsp: ENST00000589404.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19580
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7953
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19708
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35269
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr141Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

17-34871826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871826
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871826
    reference: chr 17
allele count: 109
allele frequency: 9.88859454947926e-4
allele num: 110228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.422C>T
  hgvsp: ENSP00000465350.1:p.Thr141Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.20C>T
  hgvsp: ENSP00000438365.1:p.Thr7Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.422C>T
  hgvsp: ENSP00000467285.1:p.Thr141Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.422C>T
  hgvsp: ENSP00000268852.8:p.Thr141Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.422C>T
  hgvsp: ENSP00000468792.1:p.Thr141Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.422C>T
  hgvsp: ENSP00000409936.2:p.Thr141Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.422C>T
  hgvsp: ENSP00000468488.1:p.Thr141Met
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.422C>T
  hgvsp: ENSP00000466786.1:p.Thr141Met
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18880
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18922
  bin: 2.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1899
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32813
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr141Met
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS

17-34871830-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871830
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871830
    reference: chr 17
allele count: 21
allele frequency: 1.916687963199591e-4
allele num: 109564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.418T>A
  hgvsp: ENSP00000468792.1:p.Trp140Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.418T>A
  hgvsp: ENSP00000409936.2:p.Trp140Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.16T>A
  hgvsp: ENSP00000438365.1:p.Trp6Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.418T>A
  hgvsp: ENSP00000467285.1:p.Trp140Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.418T>A
  hgvsp: ENSP00000468488.1:p.Trp140Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.418T>A
  hgvsp: ENSP00000466786.1:p.Trp140Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.418T>A
  hgvsp: ENSP00000465350.1:p.Trp140Arg
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.418T>A
  hgvsp: ENSP00000268852.8:p.Trp140Arg
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18674
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9870
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33210
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11799
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Trp140Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

17-34871831-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871831
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871831
    reference: chr 17
allele count: 1
allele frequency: 9.150805270863836e-6
allele num: 109280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.15A>G
  hgvsp: ENST00000544606.1:c.15A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.417A>G
  hgvsp: ENST00000586007.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.417A>G
  hgvsp: ENST00000589404.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.417A>G
  hgvsp: ENST00000585719.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.417A>G
  hgvsp: ENST00000268852.9:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.417A>G
  hgvsp: ENST00000431794.3:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.417A>G
  hgvsp: ENST00000586908.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.417A>G
  hgvsp: ENST00000591794.1:c.417A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 9.75e1
  variant carriers: 1
hgvs: c.417A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ

17-34871837-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871837
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871837
    reference: chr 17
allele count: 4
allele frequency: 3.72425607984805e-5
allele num: 107404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-4A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-4A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-4A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-4A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-4A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-4A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-4A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-4A>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16329
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2859
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14845
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
hgvs: c.415-4A>T
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ

17-34871839-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871839
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871839
    reference: chr 17
allele count: 4
allele frequency: 3.764139047296407e-5
allele num: 106266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-6C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-6C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-6C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-6C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-6C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-6C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-6C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-6C>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14961
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
hgvs: c.415-6C>T
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

17-34871848-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871848
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871848
    reference: chr 17
allele count: 18
allele frequency: 1.732801940738174e-4
allele num: 103878
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-15C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-15C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-15C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-15C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-15C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-15C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-15C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-15C>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19792
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11507
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11532
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4402
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 2189
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

17-34871850-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871850
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871850
    reference: chr 17
allele count: 1
allele frequency: 9.710434833271834e-6
allele num: 102982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-17G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-17G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-17G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-17G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-17G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-17G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-17G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-17G>A
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5371
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20770
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

17-34871852-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871852
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871852
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 102256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-19A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-19A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-19A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-19A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-19A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-19A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-19A>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-19A>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5975
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5933
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15429
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

17-34871852-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871852
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871852
    reference: chr 17
allele count: 4
allele frequency: 3.911750899702707e-5
allele num: 102256
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-19A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-19A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-19A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-19A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-19A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-19A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-19A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-19A>G
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5975
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9204
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5277
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2789
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 15429
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

17-34871859-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871859
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871859
    reference: chr 17
allele count: 2
allele frequency: 1.988229680292667e-5
allele num: 100592
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-26C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-26C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-26C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-26C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-26C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-26C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-26C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-26C>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6987
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24820
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3458
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22440
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7069
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

17-34871859-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871859
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871859
    reference: chr 17
allele count: 1
allele frequency: 9.941148401463337e-6
allele num: 100592
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-26C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-26C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-26C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-26C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-26C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-26C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-26C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-26C>G
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24820
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3458
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7069
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

17-34871862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871862
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871862
    reference: chr 17
allele count: 8
allele frequency: 8.041170794467674e-5
allele num: 99488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-29C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-29C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-29C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-29C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-29C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-29C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-29C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-29C>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5412
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9111
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25663
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9115
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6067
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22662
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1463
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6295
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

17-34871863-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871863
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871863
    reference: chr 17
allele count: 1
allele frequency: 1.00767851024809e-5
allele num: 99238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-30A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-30A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-30A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-30A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-30A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-30A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-30A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-30A>G
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22687
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6401
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-34871875-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871875
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871875
    reference: chr 17
allele count: 2
allele frequency: 2.192742023900888e-5
allele num: 91210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-42G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-42G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-42G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-42G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-42G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-42G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-42G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-42G>A
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12418
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13176
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23808
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9037
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2723
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2065
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6673
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP

17-34871876-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871876
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871876
    reference: chr 17
allele count: 24
allele frequency: 2.704042543602686e-4
allele num: 88756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-43C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-43C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-43C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-43C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-43C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-43C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-43C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-43C>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23183
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12988
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2871
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6558
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1418
  bin: 9.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 2466
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3622
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/17-34871877-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871877
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871877
    reference: chr 17
allele count: 1
allele frequency: 1.115822361080116e-5
allele num: 89620
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-44G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-44G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-44G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-44G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-44G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-44G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-44G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-44G>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23236
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12842
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18659
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5777
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2862
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/17-34871878-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34871878
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34871878
    reference: chr 17
allele count: 2
allele frequency: 2.252150804017837e-5
allele num: 88804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.415-45G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.415-45G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.415-45G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.13-45G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.415-45G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.415-45G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.415-45G>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.415-45G>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12786
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2540
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2059
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2854
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9111
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

17-34881016-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881016
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881016
    reference: chr 17
allele count: 2
allele frequency: 1.677852348993288e-5
allele num: 119200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+43G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+43G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7341G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+43G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+43G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+43G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+43G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+43G>A
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4933
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1943
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-34881023-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881023
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881023
    reference: chr 17
allele count: 1
allele frequency: 8.376893177858196e-6
allele num: 119376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+36A>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7334A>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+36A>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+36A>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+36A>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+36A>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+36A>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+36A>C
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4031
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

17-34881024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881024
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881024
    reference: chr 17
allele count: 12
allele frequency: 1.005918151793049e-4
allele num: 119294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+35G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+35G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+35G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7333G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+35G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+35G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+35G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+35G>A
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

17-34881025-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881025
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881025
    reference: chr 17
allele count: 5
allele frequency: 4.189359028068705e-5
allele num: 119350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+34C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+34C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+34C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7332C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+34C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+34C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+34C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+34C>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

17-34881027-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881027
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881027
    reference: chr 17
allele count: 1
allele frequency: 8.373105584861425e-6
allele num: 119430
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+32C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7330C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+32C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+32C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+32C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+32C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+32C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+32C>G
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1542
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

17-34881037-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881037
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881037
    reference: chr 17
allele count: 1
allele frequency: 8.360085607276618e-6
allele num: 119616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+22C>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+22C>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+22C>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7320C>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+22C>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+22C>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+22C>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+22C>A
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4930
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

17-34881039-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881039
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881039
    reference: chr 17
allele count: 2
allele frequency: 1.67117884956048e-5
allele num: 119676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+20A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+20A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7318A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+20A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+20A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+20A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+20A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+20A>G
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44727
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

17-34881046-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881046
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881046
    reference: chr 17
allele count: 2
allele frequency: 1.668251505596984e-5
allele num: 119886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+13C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+13C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7311C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+13C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+13C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+13C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+13C>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+13C>G
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6067
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

17-34881047-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881047
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881047
    reference: chr 17
allele count: 1
allele frequency: 8.337363058811759e-6
allele num: 119942
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+12T>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+12T>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+12T>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+12T>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+12T>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7310T>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+12T>C
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+12T>C
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1577
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

17-34881047-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881047
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881047
    reference: chr 17
allele count: 9
allele frequency: 7.503626752930583e-5
allele num: 119942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+12T>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+12T>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7310T>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+12T>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+12T>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+12T>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+12T>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+12T>A
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4931
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6069
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

17-34881048-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881048
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881048
    reference: chr 17
allele count: 1
allele frequency: 8.3380582329987e-6
allele num: 119932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+11G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+11G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+11G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+11G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+11G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7309G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+11G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+11G>A
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4933
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6059
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

17-34881049-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881049
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881049
    reference: chr 17
allele count: 4
allele frequency: 3.332611267558696e-5
allele num: 120026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414+10C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414+10C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414+10C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414+10C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7308C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414+10C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414+10C>T
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414+10C>T
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4933
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1660
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6329
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-34881059-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881059
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881059
    reference: chr 17
allele count: 1
allele frequency: 8.307717869901138e-6
allele num: 120370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.414G>A
  hgvsp: ENST00000591794.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.414G>A
  hgvsp: ENST00000586007.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.414G>A
  hgvsp: ENST00000589404.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.414G>A
  hgvsp: ENST00000268852.9:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.414G>A
  hgvsp: ENST00000431794.3:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.414G>A
  hgvsp: ENST00000585719.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7298G>A
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.414G>A
  hgvsp: ENST00000586908.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 7.75e1
  variant carriers: 0
hgvs: c.414G>A
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-34881070-C-CAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881070
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881072
    reference: chr 17
allele count: 1
allele frequency: 8.295175525914129e-6
allele num: 120552
alternate allele: CAG
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.402_403insCT
  hgvsp: ENSP00000465350.1:p.Gly135LeufsTer12
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.402_403insCT
  hgvsp: ENSP00000268852.8:p.Gly135LeufsTer12
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.402_403insCT
  hgvsp: ENSP00000468488.1:p.Gly135LeufsTer12
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.402_403insCT
  hgvsp: ENSP00000467285.1:p.Gly135LeufsTer12
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7286_12+7287insCT
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.402_403insCT
  hgvsp: ENSP00000466786.1:p.Gly135LeufsTer12
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.402_403insCT
  hgvsp: ENSP00000468792.1:p.Gly135LeufsTer12
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.402_403insCT
  hgvsp: ENSP00000409936.2:p.Gly135LeufsTer12
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1582
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly135LeufsTer12
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

17-34881073-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881073
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881073
    reference: chr 17
allele count: 1
allele frequency: 8.291186468783682e-6
allele num: 120610
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7284A>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.400A>G
  hgvsp: ENSP00000465350.1:p.Ser134Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.400A>G
  hgvsp: ENSP00000409936.2:p.Ser134Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.400A>G
  hgvsp: ENSP00000468488.1:p.Ser134Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.400A>G
  hgvsp: ENSP00000268852.8:p.Ser134Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.400A>G
  hgvsp: ENSP00000467285.1:p.Ser134Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.400A>G
  hgvsp: ENSP00000466786.1:p.Ser134Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.400A>G
  hgvsp: ENSP00000468792.1:p.Ser134Gly
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4932
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1755
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser134Gly
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

17-34881083-GACA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881083
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881080
    reference: chr 17
allele count: 5
allele frequency: 4.142982616044943e-5
allele num: 120686
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.387_389delTGT
  hgvsp: ENSP00000467285.1:p.Val130del
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.387_389delTGT
  hgvsp: ENSP00000468488.1:p.Val130del
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.387_389delTGT
  hgvsp: ENSP00000409936.2:p.Val130del
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.387_389delTGT
  hgvsp: ENSP00000468792.1:p.Val130del
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7271_12+7273delTGT
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.387_389delTGT
  hgvsp: ENSP00000466786.1:p.Val130del
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.387_389delTGT
  hgvsp: ENSP00000268852.8:p.Val130del
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.387_389delTGT
  hgvsp: ENSP00000465350.1:p.Val130del
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5455
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7137
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val130del
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: GACA
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/17-34881084-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881084
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881084
    reference: chr 17
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.389T>G
  hgvsp: ENSP00000467285.1:p.Val130Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.389T>G
  hgvsp: ENSP00000468792.1:p.Val130Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.389T>G
  hgvsp: ENSP00000468488.1:p.Val130Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.389T>G
  hgvsp: ENSP00000466786.1:p.Val130Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.389T>G
  hgvsp: ENSP00000268852.8:p.Val130Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.389T>G
  hgvsp: ENSP00000465350.1:p.Val130Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.389T>G
  hgvsp: ENSP00000409936.2:p.Val130Gly
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7273T>G
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4929
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val130Gly
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/17-34881086-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34881086
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 34881086
    reference: chr 17
allele count: 2
allele frequency: 1.657055743355207e-5
allele num: 120696
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000268852
  ensembl transcript: ENST00000268852
  gene symbol: MYO19
  hgvsc: ENST00000268852.9:c.387T>G
  hgvsp: ENST00000268852.9:c.387T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000465350
  ensembl transcript: ENST00000585719
  gene symbol: MYO19
  hgvsc: ENST00000585719.1:c.387T>G
  hgvsp: ENST00000585719.1:c.387T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000409936
  ensembl transcript: ENST00000431794
  gene symbol: MYO19
  hgvsc: ENST00000431794.3:c.387T>G
  hgvsp: ENST00000431794.3:c.387T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000466786
  ensembl transcript: ENST00000586007
  gene symbol: MYO19
  hgvsc: ENST00000586007.1:c.387T>G
  hgvsp: ENST00000586007.1:c.387T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000467285
  ensembl transcript: ENST00000589404
  gene symbol: MYO19
  hgvsc: ENST00000589404.1:c.387T>G
  hgvsp: ENST00000589404.1:c.387T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468488
  ensembl transcript: ENST00000591794
  gene symbol: MYO19
  hgvsc: ENST00000591794.1:c.387T>G
  hgvsp: ENST00000591794.1:c.387T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000438365
  ensembl transcript: ENST00000544606
  gene symbol: MYO19
  hgvsc: ENST00000544606.1:c.12+7271T>G
  variant of: http://identifiers.org/hgnc/26234
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141140
  ensembl protein: ENSP00000468792
  ensembl transcript: ENST00000586908
  gene symbol: MYO19
  hgvsc: ENST00000586908.1:c.387T>G
  hgvsp: ENST00000586908.1:c.387T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26234
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4928
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val129Val
num of homozygotes: 0
population: Other
population: African
population: East Asian
reference allele: A

GenotypeQuality
all individuals: 291
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38920
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6909
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4341
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 876
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.322340919647004e-4
allele num: 8612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66290
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

DP
type: SiteQuality
SIO_000300: 1.649116e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.138e0

VQSLOD
type: SiteQuality
SIO_000300: 1.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

QD
type: SiteQuality
SIO_000300: 1.289e1

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4342
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1531
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15916
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

QD
type: SiteQuality
SIO_000300: 1.507e1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

FS
type: SiteQuality
SIO_000300: 1.093e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 1.653656e6

MQRankSum
type: SiteQuality
SIO_000300: -3.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.98e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

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

GenotypeQuality
all individuals: 39672
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2197
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505706628120577e-5
allele num: 66414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16008
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.73e0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.191e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.12e-1

DP
type: SiteQuality
SIO_000300: 1.656018e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.064e0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2531
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505389293671343e-5
allele num: 66428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -7.580000000000001e-2

FS
type: SiteQuality
SIO_000300: 4.096e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.507e1

DP
type: SiteQuality
SIO_000300: 1.65675e6

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6980
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1535
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4355
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 701
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73370319001387e-4
allele num: 11536
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 1.65925e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.134e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

GenotypeQuality
all individuals: 39735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 516
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2190
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.330331559557921e-3
allele num: 9772
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66452
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

DP
type: SiteQuality
SIO_000300: 1.65925e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.134e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1537
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2189
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4344
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6971
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66462
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.194251734390486e-5
allele num: 16144
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.271e0

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -5.72e-2

QD
type: SiteQuality
SIO_000300: 1.323e1

MQ
type: SiteQuality
SIO_000300: 5.899e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 1.659452e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.453e0

GenotypeQuality
all individuals: 2191
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4348
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 704
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39908
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.321262766945218e-4
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

DP
type: SiteQuality
SIO_000300: 1.660757e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

QD
type: SiteQuality
SIO_000300: 1.119e1

FS
type: SiteQuality
SIO_000300: 2.068e0

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

GenotypeQuality
all individuals: 6977
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4348
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 123
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 879
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504347564461293e-5
allele num: 66474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.576e0

DP
type: SiteQuality
SIO_000300: 1.661154e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: -1.038e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.81e-1

QD
type: SiteQuality
SIO_000300: 6.36e0

GenotypeQuality
all individuals: 6970
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1533
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.023960679909891e-4
allele num: 9766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

DP
type: SiteQuality
SIO_000300: 1.661239e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

QD
type: SiteQuality
SIO_000300: 1.299e1

GenotypeQuality
all individuals: 1770
bin: 7.25e1
variant carriers: 13

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 164
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 38078
bin: 6.25e1
variant carriers: 6

GenotypeQuality
all individuals: 129
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1870
bin: 7.75e1
variant carriers: 11

GenotypeQuality
all individuals: 9267
bin: 9.75e1
variant carriers: 7000

GenotypeQuality
all individuals: 503
bin: 9.25e1
variant carriers: 22

GenotypeQuality
all individuals: 384
bin: 8.75e1
variant carriers: 11

GenotypeQuality
all individuals: 117
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 826
allele frequency: 1.250378443838934e-1
allele num: 6606
num of homozygotes: 60

East Asian
type: Population
allele count: 1504
allele frequency: 1.750058180125669e-1
allele num: 8594
num of homozygotes: 137

Other
type: Population
allele count: 70
allele frequency: 7.900677200902935e-2
allele num: 886
num of homozygotes: 4

Latino
type: Population
allele count: 365
allele frequency: 3.166753427034531e-2
allele num: 11526
num of homozygotes: 6

African
type: Population
allele count: 87
allele frequency: 8.910282671036461e-3
allele num: 9764
num of homozygotes: 0

South Asian
type: Population
allele count: 1182
allele frequency: 7.263119085658105e-2
allele num: 16274
num of homozygotes: 48

European (Non-Finnish)
type: Population
allele count: 3413
allele frequency: 5.131404859273515e-2
allele num: 66512
num of homozygotes: 85

DP
type: SiteQuality
SIO_000300: 1.789795e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.92e0

QD
type: SiteQuality
SIO_000300: 1.475e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1137
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42946
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 530
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.140243153628883e-5
allele num: 16286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.615297e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.429999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.532e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.998e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

FS
type: SiteQuality
SIO_000300: 6.377e0

QD
type: SiteQuality
SIO_000300: 9.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 240
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 521
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1119
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504800312998465e-5
allele num: 66454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.612813e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.298e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-2

QD
type: SiteQuality
SIO_000300: 7.52e0

VQSLOD
type: SiteQuality
SIO_000300: -1.07e0

GenotypeQuality
all individuals: 462
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42196
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 4.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505072092953252e-5
allele num: 66442
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.296e0

MQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

FS
type: SiteQuality
SIO_000300: 6.449e0

QD
type: SiteQuality
SIO_000300: 1.453e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 1.611636e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.07e-1

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7013
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2016
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42196
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505072092953252e-5
allele num: 66442
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.296e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.74e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 6.449e0

DP
type: SiteQuality
SIO_000300: 1.611636e6

MQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 1.453e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.07e-1

GenotypeQuality
all individuals: 287
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7007
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2470
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2098
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 8.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.739130434782609e-4
allele num: 11500
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 3.507e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.103e0

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.288e1

DP
type: SiteQuality
SIO_000300: 1.611814e6

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

GenotypeQuality
all individuals: 217
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2469
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2000
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.134969325153375e-5
allele num: 16300
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66444
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.122e0

VQSLOD
type: SiteQuality
SIO_000300: -7.099999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.356e0

QD
type: SiteQuality
SIO_000300: 9.49e0

DP
type: SiteQuality
SIO_000300: 1.610776e6

GenotypeQuality
all individuals: 6916
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 285
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2467
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 320
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1090
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66386
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16282
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.695e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

DP
type: SiteQuality
SIO_000300: 1.608022e6

QD
type: SiteQuality
SIO_000300: 3.023e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.249e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 960
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2041
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6828
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66332
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.128668171557562e-3
allele num: 886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 1.335e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.01e-1

FS
type: SiteQuality
SIO_000300: 1.279e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.603307e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.31e-1

GenotypeQuality
all individuals: 366
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1066
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41857
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9696
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66256
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.166044776119403e-4
allele num: 8576
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

FS
type: SiteQuality
SIO_000300: 1.121e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 1.598142e6

QD
type: SiteQuality
SIO_000300: 1.221e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.275e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.86e-1

GenotypeQuality
all individuals: 77
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41799
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1932
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2015
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2463
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6700
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16174
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.031778786628147e-4
allele num: 9692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66230
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.596979e6

VQSLOD
type: SiteQuality
SIO_000300: -3.525e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.82e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.444e1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

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

GenotypeQuality
all individuals: 533
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 408
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 726
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2458
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1837
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.2453300124533e-4
allele num: 16060
num of homozygotes: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

QD
type: SiteQuality
SIO_000300: 1.573e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

DP
type: SiteQuality
SIO_000300: 1.579882e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

FS
type: SiteQuality
SIO_000300: 1.201e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1837
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1771
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2458
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 6428
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 485
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.9813200498132e-4
allele num: 16060
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.067777069870453e-5
allele num: 65922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.579882e6

FS
type: SiteQuality
SIO_000300: 1.201e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

QD
type: SiteQuality
SIO_000300: 1.573e1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1851
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40344
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2445
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11280
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.248437890527369e-5
allele num: 16004
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.572e0

VQSLOD
type: SiteQuality
SIO_000300: -3.481e-1

QD
type: SiteQuality
SIO_000300: 8.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.079e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.175e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 1.575177e6

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

GenotypeQuality
all individuals: 621
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 690
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11164
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.054834275240568e-5
allele num: 65470
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.774e0

DP
type: SiteQuality
SIO_000300: 1.556177e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

QD
type: SiteQuality
SIO_000300: 1.077e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1684
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2803
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2433
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 923
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5838
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39708
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.537515375153752e-4
allele num: 6504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15860
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.933e1

VQSLOD
type: SiteQuality
SIO_000300: 3.25e-1

DP
type: SiteQuality
SIO_000300: 1.55069e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 1.417e1

MQRankSum
type: SiteQuality
SIO_000300: -2.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

FS
type: SiteQuality
SIO_000300: 4.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

GenotypeQuality
all individuals: 1611
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2432
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 463
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1669
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11116
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.307556452630251e-5
allele num: 15854
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.75e0

DP
type: SiteQuality
SIO_000300: 1.550806e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.143e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 4.71e0

MQRankSum
type: SiteQuality
SIO_000300: -1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.61e-1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2429
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2899
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40310
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5780
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531205977828137e-5
allele num: 65308
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11106
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.154e0

QD
type: SiteQuality
SIO_000300: 1.399e1

DP
type: SiteQuality
SIO_000300: 1.54955e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: 2.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

GenotypeQuality
all individuals: 1469
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2566
bin: 9.75e1
variant carriers: 163

GenotypeQuality
all individuals: 612
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40287
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 4.540501271340356e-4
allele num: 11012
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.095996646405366e-4
allele num: 9542
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

South Asian
type: Population
allele count: 22
allele frequency: 1.399491094147583e-3
allele num: 15720
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 135
allele frequency: 2.078585945679621e-3
allele num: 64948
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.406e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

DP
type: SiteQuality
SIO_000300: 1.537618e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

FS
type: SiteQuality
SIO_000300: 5.570000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

GenotypeQuality
all individuals: 598
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37780
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1475
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5075
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 878
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.113718030014796e-4
allele num: 9462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63886
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.78e-1

QD
type: SiteQuality
SIO_000300: 1.729e1

DP
type: SiteQuality
SIO_000300: 1.496859e6

FS
type: SiteQuality
SIO_000300: 1.074e0

VQSLOD
type: SiteQuality
SIO_000300: -1.182e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.09e-1

GenotypeQuality
all individuals: 591
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 997
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 718
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 27

GenotypeQuality
all individuals: 1113
bin: 7.75e1
variant carriers: 18

GenotypeQuality
all individuals: 444
bin: 5.75e1
variant carriers: 7

GenotypeQuality
all individuals: 5575
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 5976
bin: 9.75e1
variant carriers: 4597

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1101
bin: 7.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1012
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 571
bin: 8.25e1
variant carriers: 13

South Asian
type: Population
allele count: 243
allele frequency: 1.576284379865075e-2
allele num: 15416
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 2406
allele frequency: 3.774472891566265e-2
allele num: 63744
num of homozygotes: 43

Other
type: Population
allele count: 27
allele frequency: 3.20665083135392e-2
allele num: 842
num of homozygotes: 1

East Asian
type: Population
allele count: 173
allele frequency: 2.083835220428812e-2
allele num: 8302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 237
allele frequency: 3.75e-2
allele num: 6320
num of homozygotes: 3

African
type: Population
allele count: 1542
allele frequency: 1.632437010374762e-1
allele num: 9446
num of homozygotes: 109

Latino
type: Population
allele count: 248
allele frequency: 2.311707680835198e-2
allele num: 10728
num of homozygotes: 2

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

QD
type: SiteQuality
SIO_000300: 1.555e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.98e-2

FS
type: SiteQuality
SIO_000300: 1.227e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e-1

DP
type: SiteQuality
SIO_000300: 1.521844e6

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4473
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 747
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 574
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 583
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 37321
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 455
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7594
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6220
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.598046978094485e-5
allele num: 15156
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.403846153846154e-3
allele num: 832
num of homozygotes: 0

African
type: Population
allele count: 713
allele frequency: 7.766884531590414e-2
allele num: 9180
num of homozygotes: 32

European (Non-Finnish)
type: Population
allele count: 35
allele frequency: 5.577867023650157e-4
allele num: 62748
num of homozygotes: 0

Latino
type: Population
allele count: 38
allele frequency: 3.595760787282362e-3
allele num: 10568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.52e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

DP
type: SiteQuality
SIO_000300: 1.424076e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.007e0

QD
type: SiteQuality
SIO_000300: 1.328e1

FS
type: SiteQuality
SIO_000300: 1.245e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1070
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37423
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7971
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4429
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62558
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.620762711864407e-5
allele num: 15104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8184
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 1.407901e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

GenotypeQuality
all individuals: 7971
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1372
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15104
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.665689149560117e-4
allele num: 8184
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

QD
type: SiteQuality
SIO_000300: 9.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

DP
type: SiteQuality
SIO_000300: 1.407901e6

GenotypeQuality
all individuals: 556
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36131
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4282
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1425
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 465
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62120
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.672597864768683e-4
allele num: 8992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.973e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.380641e6

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.963e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.131e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

GenotypeQuality
all individuals: 163
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9789
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4194
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 1662
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 8.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14902
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.678668215253581e-5
allele num: 10332
num of homozygotes: 0

African
type: Population
allele count: 30
allele frequency: 3.35795836131632e-3
allele num: 8934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.346e1

DP
type: SiteQuality
SIO_000300: 1.367573e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e-1

GenotypeQuality
all individuals: 10770
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3861
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 9.75e1
variant carriers: 110

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

GenotypeQuality
all individuals: 1918
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.780907668231612e-5
allele num: 10224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8872
num of homozygotes: 0

South Asian
type: Population
allele count: 108
allele frequency: 7.304206681996483e-3
allele num: 14786
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8030
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

QD
type: SiteQuality
SIO_000300: 1.215e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.39e0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

DP
type: SiteQuality
SIO_000300: 1.345219e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2021
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3697
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2079
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 2.265005662514156e-4
allele num: 8830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.785697899256055e-4
allele num: 61026
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.858044164037855e-5
allele num: 10144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14682
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.222493887530562e-3
allele num: 818
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

QD
type: SiteQuality
SIO_000300: 1.338e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.322414e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 193
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3673
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32908
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2099
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.255965837729214e-4
allele num: 7962
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14644
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

FS
type: SiteQuality
SIO_000300: 6.141e0

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.56e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

QD
type: SiteQuality
SIO_000300: 8.279999999999999e0

DP
type: SiteQuality
SIO_000300: 1.314325e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2766
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29282
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 408
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2765
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7822
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8676
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.036326942482341e-4
allele num: 9910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59856
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 6.326e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.2545e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.99e-1

QD
type: SiteQuality
SIO_000300: 9.84e0

MQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26284
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16266
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3198
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3213
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.026061974143238e-4
allele num: 9746
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5896
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.020499859590003e-5
allele num: 14244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.375185635209936e-5
allele num: 59256
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.219669e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.75e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

QD
type: SiteQuality
SIO_000300: 8.789999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -5.545e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.586e0

FS
type: SiteQuality
SIO_000300: 1.4669e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 19721
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 20517
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 168
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4666
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 18
allele frequency: 2.134218638842779e-3
allele num: 8434
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13914
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.272e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

DP
type: SiteQuality
SIO_000300: 1.124143e6

QD
type: SiteQuality
SIO_000300: 1.262e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

GenotypeQuality
all individuals: 556
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4905
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17914
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2492
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13740
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5734
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.738465282848302e-5
allele num: 57522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.509e1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.664e0

MQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

FS
type: SiteQuality
SIO_000300: 1.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 1.088195e6

GenotypeQuality
all individuals: 1409
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21413
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 480
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5277
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5712
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

FS
type: SiteQuality
SIO_000300: 7.548e0

DP
type: SiteQuality
SIO_000300: 1.058194e6

VQSLOD
type: SiteQuality
SIO_000300: 4.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.799e0

QD
type: SiteQuality
SIO_000300: 9.58e0

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5933
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21413
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5712
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13628
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8278
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.317789291882556e-4
allele num: 9264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57162
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.799e0

QD
type: SiteQuality
SIO_000300: 9.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.23e-1

FS
type: SiteQuality
SIO_000300: 7.548e0

VQSLOD
type: SiteQuality
SIO_000300: 4.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

DP
type: SiteQuality
SIO_000300: 1.058194e6

GenotypeQuality
all individuals: 1554
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5948
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12703
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8166
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.554291807357384e-5
allele num: 56270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13368
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.164e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.698e0

DP
type: SiteQuality
SIO_000300: 1.00536e6

QD
type: SiteQuality
SIO_000300: 1.026e1

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-1

GenotypeQuality
all individuals: 12703
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5948
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22440
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13368
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.224589762429586e-4
allele num: 8166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9096
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.026e1

FS
type: SiteQuality
SIO_000300: 1.698e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.164e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 1.00536e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

GenotypeQuality
all individuals: 160
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1357
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4016
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7818
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1409
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 438
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10225
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.257183908045977e-4
allele num: 55680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8980
num of homozygotes: 0

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

African
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: 5558
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.581501137225171e-5
allele num: 13190
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.388e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.73987e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

QD
type: SiteQuality
SIO_000300: 1.195e1

MQRankSum
type: SiteQuality
SIO_000300: -3.37e-1

GenotypeQuality
all individuals: 1402
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4209
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8041
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.244400199104032e-4
allele num: 8036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13194
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.6425e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.534e0

QD
type: SiteQuality
SIO_000300: 9.800000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.976e-1

FS
type: SiteQuality
SIO_000300: 2.177e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.743e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19661
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2450
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5706
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1936
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3613
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 2.518257365902795e-4
allele num: 7942
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12100
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

FS
type: SiteQuality
SIO_000300: 3.086e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.966e1

DP
type: SiteQuality
SIO_000300: 8.87072e5

GenotypeQuality
all individuals: 745
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18150
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5763
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 390
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2042
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2213
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2655
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9008
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 5.25e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 4.815989083758077e-4
allele num: 49834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5086
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.004e1

DP
type: SiteQuality
SIO_000300: 8.78661e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.800000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.902e0

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

GenotypeQuality
all individuals: 2394
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3353
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2039
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6618
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2194
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.986965506278811e-5
allele num: 50328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7696
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7416
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 6.67e0

MQRankSum
type: SiteQuality
SIO_000300: 8.51e-1

DP
type: SiteQuality
SIO_000300: 8.7713e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.76e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.721e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.268e0

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5780
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6596
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18005
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2470
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 735
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.966955153422502e-4
allele num: 5084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.003847386983007e-5
allele num: 49904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7616
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
SIO_000300: 9.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.5e-3

FS
type: SiteQuality
SIO_000300: 3.388e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.221e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

DP
type: SiteQuality
SIO_000300: 8.75146e5

GenotypeQuality
all individuals: 3405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44730
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1563
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 958
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.041232904674423e-4
allele num: 9798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15390
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66312
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.635e-1

DP
type: SiteQuality
SIO_000300: 3.534094e6

QD
type: SiteQuality
SIO_000300: 1.63e1

MQRankSum
type: SiteQuality
SIO_000300: 4.42e-1

MQ
type: SiteQuality
SIO_000300: 5.792e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

GenotypeQuality
all individuals: 807
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1941
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4013
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1360
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44729
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507386192342478e-5
allele num: 66340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.52e-1

QD
type: SiteQuality
SIO_000300: 1.419e1

DP
type: SiteQuality
SIO_000300: 3.538419e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

GenotypeQuality
all individuals: 1558
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1941
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44729
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 749
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.459948320413436e-5
allele num: 15480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.658574831880824e-4
allele num: 66322
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.648e0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.704e0

QD
type: SiteQuality
SIO_000300: 1.396e1

DP
type: SiteQuality
SIO_000300: 3.539658e6

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

GenotypeQuality
all individuals: 97
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1943
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4364
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44725
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 50
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.030271965265633e-5
allele num: 66332
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.441638752898738e-5
allele num: 15524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

DP
type: SiteQuality
SIO_000300: 3.5408e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.191e0

QD
type: SiteQuality
SIO_000300: 1.446e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 592
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1349
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4552
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1943
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44725
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507022725902707e-5
allele num: 66356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15578
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.542601e6

FS
type: SiteQuality
SIO_000300: 4.229e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.008e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.675e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.667e1

GenotypeQuality
all individuals: 666
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1585
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5369
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44726
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 404
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15702
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505706628120577e-5
allele num: 66414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 8.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.601e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 3.551647e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

QD
type: SiteQuality
SIO_000300: 9.06e0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5585
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1354
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1587
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.269680040629761e-4
allele num: 15752
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.22e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

QD
type: SiteQuality
SIO_000300: 1.611e1

FS
type: SiteQuality
SIO_000300: 1.169e1

VQSLOD
type: SiteQuality
SIO_000300: -1.202e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-1

DP
type: SiteQuality
SIO_000300: 3.553594e6

GenotypeQuality
all individuals: 1946
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 519
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44726
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1577
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1357
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.559813e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.387e0

FS
type: SiteQuality
SIO_000300: 1.212e0

VQSLOD
type: SiteQuality
SIO_000300: 8.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.649e1

GenotypeQuality
all individuals: 1631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6069
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44729
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1946
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.276675872457946e-5
allele num: 15932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 4.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.372e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 3.561115e6

QD
type: SiteQuality
SIO_000300: 1.24e1

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44729
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.203007518796992e-4
allele num: 66500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15932
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

QD
type: SiteQuality
SIO_000300: 1.24e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.372e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.37e0

DP
type: SiteQuality
SIO_000300: 3.561115e6

GenotypeQuality
all individuals: 1624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1573
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44724
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.280618012812461e-5
allele num: 15922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.654e0

VQSLOD
type: SiteQuality
SIO_000300: -2.11e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.119e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 3.561736e6

MQRankSum
type: SiteQuality
SIO_000300: 9.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.1e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

QD
type: SiteQuality
SIO_000300: 1.312e1

GenotypeQuality
all individuals: 962
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44724
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 4
allele frequency: 4.079967360261118e-4
allele num: 9804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.563066e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

QD
type: SiteQuality
SIO_000300: 1.433e1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

FS
type: SiteQuality
SIO_000300: 2.379e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44724
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6800
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

QD
type: SiteQuality
SIO_000300: 1.154e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.271e0

DP
type: SiteQuality
SIO_000300: 3.570186e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.951e0

GenotypeQuality
all individuals: 44725
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1946
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 966
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6990
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.349e0

MQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.75e-1

DP
type: SiteQuality
SIO_000300: 3.573575e6

QD
type: SiteQuality
SIO_000300: 1.889e1

GenotypeQuality
all individuals: 112
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7076
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1947
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1373
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 791
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44725
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1581
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 3.574138e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

FS
type: SiteQuality
SIO_000300: 3.573e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQRankSum
type: SiteQuality
SIO_000300: -6.61e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 4.19e-1

QD
type: SiteQuality
SIO_000300: 1.574e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.3e-1

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1949
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44727
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1575
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.427773731488225e-4
allele num: 16476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQ
type: SiteQuality
SIO_000300: 5.819e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.71e-1

FS
type: SiteQuality
SIO_000300: 1.92e0

QD
type: SiteQuality
SIO_000300: 1.17e1

MQRankSum
type: SiteQuality
SIO_000300: -1.042e0

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-2

DP
type: SiteQuality
SIO_000300: 3.575599e6

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1364
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7145
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44722
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1949
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

FS
type: SiteQuality
SIO_000300: 9.73e-1

QD
type: SiteQuality
SIO_000300: 1.232e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.83e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 3.575188e6

GenotypeQuality
all individuals: 1949
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1770
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7160
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44726
bin: 9.75e1
variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

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