19-50764005-C-CGTGT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764005
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764009
    reference: chr 19
allele count: 1602
allele frequency: 2.060768221461833e-2
allele num: 77738
alternate allele: CGTGT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+43_2325+46dupTGTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+43_2400+46dupTGTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+43_2424+46dupTGTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+43_2424+46dupTGTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+43_2325+46dupTGTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+43_2301+46dupTGTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+43_2325+46dupTGTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+43_2424+46dupTGTG
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 2.25e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 3.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 1.75e1
  variant carriers: 453
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 2.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 7.5e0
  variant carriers: 245
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14822
  bin: 1.25e1
  variant carriers: 591
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 9.75e1
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 1.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 8.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 6.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 8.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 4.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1749
  bin: 1.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 5440
  bin: 2.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 9.25e1
  variant carriers: 33
num of homozygotes: 7
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum

19-50764005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764005
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764005
    reference: chr 19
allele count: 6
allele frequency: 7.718233039182896e-5
allele num: 77738
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+33C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+33C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+33C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+33C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+33C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+33C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+33C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+33C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14822
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1749
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8220
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

19-50764005-CGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764005
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764003
    reference: chr 19
allele count: 456
allele frequency: 5.865857109779001e-3
allele num: 77738
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+45_2424+46delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+45_2325+46delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+45_2400+46delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+45_2424+46delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+45_2325+46delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+45_2424+46delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+45_2325+46delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+45_2301+46delTG
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14822
  bin: 1.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 2.25e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 3.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 1.75e1
  variant carriers: 151
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 2.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 7.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 1749
  bin: 1.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 5440
  bin: 2.5e0
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 8.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 7034
  bin: 2.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 21289
  bin: 9.75e1
  variant carriers: 74
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 9.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 6.25e1
  variant carriers: 46
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: CGT
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

19-50764005-CGTGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764005
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764001
    reference: chr 19
allele count: 1
allele frequency: 1.286372173197149e-5
allele num: 77738
alternate allele: C
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14822
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7034
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5440
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21289
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1749
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8220
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 43692
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 12404
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5990
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 5024
  num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
reference allele: CGTGT
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

19-50764012-GTGTGTGCGTGCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764012
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764000
    reference: chr 19
allele count: 1
allele frequency: 1.445504481063891e-5
allele num: 69180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13987
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3603
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2931
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1059
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7015
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4826
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: GTGTGTGCGTGCA
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-50764013-T-TGTGCGCGTGCATGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764013
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764027
    reference: chr 19
allele count: 2
allele frequency: 2.870346450816614e-5
allele num: 69678
alternate allele: TGTGCGCGTGCATGA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13932
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4849
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4602
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12116
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3343
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3950
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

19-50764013-T-TGTGTGCGCGTGCATGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764013
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764029
    reference: chr 19
allele count: 277
allele frequency: 3.97542983438101e-3
allele num: 69678
alternate allele: TGTGTGCGCGTGCATGA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 2.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 7.5e0
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 13272
  bin: 1.25e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13932
  bin: 1.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 2.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6963
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3602
  bin: 2.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3193
  bin: 9.75e1
  variant carriers: 306
genotype quality: GenotypeQuality
  all individuals: 3950
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4849
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1042
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12116
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 3
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

19-50764013-TGTGTGCGTGCATGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764013
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50763999
    reference: chr 19
allele count: 4
allele frequency: 5.740692901633227e-5
allele num: 69678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13272
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13932
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3950
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2605
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3193
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6963
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4849
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3343
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: TGTGTGCGTGCATGA
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

19-50764015-T-TGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764015
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764017
    reference: chr 19
allele count: 17
allele frequency: 2.568286197727822e-4
allele num: 66192
alternate allele: TGC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+44_2424+45insCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+44_2424+45insCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+44_2301+45insCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+44_2400+45insCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+44_2325+45insCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+44_2325+45insCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+44_2424+45insCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+44_2325+45insCG
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13149
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13910
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 10536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3480
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3837
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4914
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum

19-50764015-TGTGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764015
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764011
    reference: chr 19
allele count: 10
allele frequency: 1.510756586898719e-4
allele num: 66192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+48_2424+51delGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+48_2325+51delGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+48_2301+51delGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+48_2400+51delGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+48_2325+51delGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+48_2424+51delGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+48_2325+51delGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+48_2424+51delGTGC
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13910
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13149
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3929
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3480
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2975
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3837
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6857
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4914
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: TGTGC
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

19-50764015-TGTGCGTGCATGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764015
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764003
    reference: chr 19
allele count: 6
allele frequency: 9.064539521392314e-5
allele num: 66192
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13910
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13149
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6857
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2975
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3480
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3929
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4914
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6162
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2946
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3837
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 37878
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3120
  num of homozygotes: 0
population: African
  type: Population
  allele count: 6
  allele frequency: 1.159644375724778e-3
  allele num: 5174
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10962
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
reference allele: TGTGCGTGCATGA
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

19-50764015-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764015
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764015
    reference: chr 19
allele count: 2
allele frequency: 3.021513173797438e-5
allele num: 66192
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+43T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+43T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+43T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+43T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+43T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+43T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+43T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+43T>C
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13910
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13149
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3837
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3929
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6162
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3480
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6857
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

19-50764015-T-TGTGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764015
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764019
    reference: chr 19
allele count: 2
allele frequency: 3.021513173797438e-5
allele num: 66192
alternate allele: TGTGC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+48_2424+51dupGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+48_2325+51dupGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+48_2325+51dupGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+48_2424+51dupGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+48_2400+51dupGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+48_2325+51dupGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+48_2424+51dupGTGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+48_2301+51dupGTGC
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13910
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4914
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 652
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 7.25e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-50764017-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764017
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764017
    reference: chr 19
allele count: 401
allele frequency: 4.31386892723439e-3
allele num: 92956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+45T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+45T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+45T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+45T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+45T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+45T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+45T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+45T>C
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 2.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16976
  bin: 1.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 7.5e0
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 14698
  bin: 1.75e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4986
  bin: 2.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 5.25e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 7.5e0
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 7.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 4.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 5.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 5538
  bin: 2.5e0
  variant carriers: 9
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

19-50764017-T-TGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764017
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764019
    reference: chr 19
allele count: 39981
allele frequency: 4.301067171565042e-1
allele num: 92956
alternate allele: TGC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+47_2325+48dupCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+47_2325+48dupCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+47_2424+48dupCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+47_2301+48dupCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+47_2400+48dupCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+47_2424+48dupCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+47_2325+48dupCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+47_2424+48dupCG
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 216
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.25e1
  variant carriers: 645
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 137
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 700
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.25e1
  variant carriers: 874
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 7.5e0
  variant carriers: 4035
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 2.75e1
  variant carriers: 1951
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.25e1
  variant carriers: 4710
genotype depth: GenotypeDepth
  all individuals: 16976
  bin: 1.25e1
  variant carriers: 10412
genotype depth: GenotypeDepth
  all individuals: 14698
  bin: 1.75e1
  variant carriers: 9016
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.75e1
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 9.75e1
  variant carriers: 673
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 445
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.25e1
  variant carriers: 364
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 685
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.25e1
  variant carriers: 600
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 8.25e1
  variant carriers: 318
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 7.5e0
  variant carriers: 324
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 9.25e1
  variant carriers: 388
genotype quality: GenotypeQuality
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 1105
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 3.75e1
  variant carriers: 1372
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 8.75e1
  variant carriers: 355
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 7.75e1
  variant carriers: 337
genotype quality: GenotypeQuality
  all individuals: 5538
  bin: 2.5e0
  variant carriers: 245
num of homozygotes: 8745
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

19-50764017-T-TGCGCGTGCATGAGTGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764017
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764033
    reference: chr 19
allele count: 1
allele frequency: 1.075777787340247e-5
allele num: 92956
alternate allele: TGCGCGTGCATGAGTGC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14698
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4986
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5538
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

19-50764017-T-TGTGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764017
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764021
    reference: chr 19
allele count: 17
allele frequency: 1.82882223847842e-4
allele num: 92956
alternate allele: TGTGC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+46_2325+47insTGCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+46_2400+47insTGCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+46_2301+47insTGCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+46_2325+47insTGCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+46_2424+47insTGCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+46_2325+47insTGCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+46_2424+47insTGCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+46_2424+47insTGCG
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14698
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16976
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5538
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

19-50764017-TGC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764017
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764015
    reference: chr 19
allele count: 3
allele frequency: 3.227333362020741e-5
allele num: 92956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+47_2325+48delCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+47_2424+48delCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+47_2325+48delCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+47_2400+48delCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+47_2325+48delCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+47_2424+48delCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+47_2301+48delCG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+47_2424+48delCG
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16976
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14698
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5538
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: TGC
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

19-50764017-TGCGTGCATGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764017
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764007
    reference: chr 19
allele count: 75
allele frequency: 8.068333405051852e-4
allele num: 92956
alternate allele: T
canonical: false
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16976
  bin: 1.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14698
  bin: 1.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3501
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5538
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4986
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24944
  bin: 9.75e1
  variant carriers: 76
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 712
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 5
  allele frequency: 9.718172983479106e-5
  allele num: 51450
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 4
  allele frequency: 4.827419744146754e-4
  allele num: 8286
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4930
  num of homozygotes: 0
population: East Asian
population: South Asian
population: African
reference allele: TGCGTGCATGA
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-50764018-G-GCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764018
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764020
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 30048
alternate allele: GCA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+47_2325+48insAC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+47_2400+48insAC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+47_2325+48insAC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+47_2325+48insAC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+47_2424+48insAC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+47_2424+48insAC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+47_2424+48insAC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+47_2301+48insAC
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 10039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3780
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

19-50764019-CGTGCATGAGTGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764019
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764007
    reference: chr 19
allele count: 1348
allele frequency: 1.56704098951431e-2
allele num: 86022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 14763
  bin: 1.75e1
  variant carriers: 265
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 3.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 16595
  bin: 1.25e1
  variant carriers: 424
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 5.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 7.5e0
  variant carriers: 276
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 2.75e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 2.25e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 2297
  bin: 1.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 8.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 2399
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 9.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 10805
  bin: 2.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 4.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 5096
  bin: 3.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 5.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 8.25e1
  variant carriers: 15
num of homozygotes: 36
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: CGTGCATGAGTGT
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-50764019-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764019
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764019
    reference: chr 19
allele count: 24
allele frequency: 2.789983957592244e-4
allele num: 86022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+47C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+47C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+47C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+47C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+47C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+47C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+47C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+47C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16595
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14763
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10805
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 7263
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5193
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2600
  bin: 7.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 5780
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 5096
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 1
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

19-50764019-CGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764019
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764017
    reference: chr 19
allele count: 1
allele frequency: 1.162493315663435e-5
allele num: 86022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+49_2424+50delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+49_2424+50delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+49_2424+50delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+49_2325+50delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+49_2325+50delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+49_2325+50delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+49_2301+50delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+49_2400+50delTG
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16595
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10805
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5193
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2655
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2032
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5188
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2337
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2297
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CGT
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

19-50764021-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764021
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764021
    reference: chr 19
allele count: 4
allele frequency: 4.506534474988734e-5
allele num: 88760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+49T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+49T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+49T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+49T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+49T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+49T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+49T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+49T>C
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17015
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14034
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7859
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9801
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 5745
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4840
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-50764021-T-TGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764021
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764023
    reference: chr 19
allele count: 2
allele frequency: 2.253267237494367e-5
allele num: 88760
alternate allele: TGC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+50_2400+51dupGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+50_2424+51dupGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+50_2301+51dupGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+50_2424+51dupGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+50_2325+51dupGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+50_2325+51dupGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+50_2325+51dupGC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+50_2424+51dupGC
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17015
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7859
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14034
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5377
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5093
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2713
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8125
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

19-50764021-TGCATGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764021
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764015
    reference: chr 19
allele count: 2
allele frequency: 2.253267237494367e-5
allele num: 88760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+51_2325+56delCATGAG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+51_2325+56delCATGAG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+51_2301+56delCATGAG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+51_2424+56delCATGAG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+51_2424+56delCATGAG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+51_2325+56delCATGAG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+51_2400+56delCATGAG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+51_2424+56delCATGAG
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14034
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17015
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5377
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2752
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2204
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5745
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1599
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: TGCATGA
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

19-50764022-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764022
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764022
    reference: chr 19
allele count: 263
allele frequency: 2.872370634105852e-3
allele num: 91562
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2301+50G>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2325+50G>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2325+50G>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2424+50G>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2400+50G>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2424+50G>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2424+50G>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2325+50G>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7935
  bin: 7.5e0
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13969
  bin: 1.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17154
  bin: 1.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 5.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5903
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4983
  bin: 1.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 2239
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5135
  bin: 9.75e1
  variant carriers: 256
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 6
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

19-50764683-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764683
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764683
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 48894
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-49C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-49C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-49C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-49C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-49C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-49C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-49C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-49C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23718
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7837
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1613
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5739
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7108
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13690
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3897
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP

19-50764684-TCCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764684
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764681
    reference: chr 19
allele count: 1
allele frequency: 2.809778027535825e-5
allele num: 35590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-45_2326-43delCCC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-45_2326-43delCCC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-45_2302-43delCCC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-45_2425-43delCCC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-45_2326-43delCCC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-45_2425-43delCCC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-45_2401-43delCCC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-45_2425-43delCCC
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6862
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7412
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23032
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6554
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: TCCC
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-50764688-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764688
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764688
    reference: chr 19
allele count: 527
allele frequency: 8.515107448699306e-3
allele num: 61890
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-44C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-44C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-44C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-44C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-44C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-44C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-44C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-44C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16809
  bin: 1.25e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 1.75e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21330
  bin: 7.5e0
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 2.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 2.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20919
  bin: 2.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4702
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 4.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2626
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 7.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6462
  bin: 3.25e1
  variant carriers: 4
num of homozygotes: 3
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

19-50764692-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764692
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764692
    reference: chr 19
allele count: 1
allele frequency: 1.34390538906061e-5
allele num: 74410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-40C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-40C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-40C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-40C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-40C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-40C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-40C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-40C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14623
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2832
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1522
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/19-50764694-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764694
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764694
    reference: chr 19
allele count: 1
allele frequency: 1.232528902802771e-5
allele num: 81134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-38C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-38C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-38C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-38C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-38C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-38C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-38C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-38C>A
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4064
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-50764697-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764697
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764697
    reference: chr 19
allele count: 1
allele frequency: 1.116669644452385e-5
allele num: 89552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-35C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-35C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-35C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-35C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-35C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-35C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-35C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-35C>A
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24706
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1557
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4070
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2879
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

19-50764698-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764698
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764698
    reference: chr 19
allele count: 3
allele frequency: 3.274823159549385e-5
allele num: 91608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-34C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-34C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-34C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-34C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-34C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-34C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-34C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-34C>G
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6650
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2563
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12340
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1390
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8256
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genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2653
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1694
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 414
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4259
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

19-50764703-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764703
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764703
    reference: chr 19
allele count: 5
allele frequency: 4.957563258507179e-5
allele num: 100856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-29C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-29C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-29C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-29C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-29C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-29C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-29C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-29C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10300
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32281
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8626
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

19-50764704-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764704
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764704
    reference: chr 19
allele count: 85
allele frequency: 8.348229193266417e-4
allele num: 101818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-28G>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-28G>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-28G>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-28G>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-28G>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-28G>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-28G>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-28G>A
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32847
  bin: 2.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10733
  bin: 2.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 36450
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4821
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7745
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

19-50764705-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764705
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764705
    reference: chr 19
allele count: 13
allele frequency: 1.244209639753455e-4
allele num: 104484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-27T>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-27T>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-27T>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-27T>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-27T>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-27T>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-27T>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-27T>A
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6771
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34267
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11214
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5324
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 6969
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-50764705-T-TCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764705
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764707
    reference: chr 19
allele count: 1
allele frequency: 9.570843382718885e-6
allele num: 104484
alternate allele: TCA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-26_2326-25dupCA
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-26_2425-25dupCA
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-26_2326-25dupCA
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-26_2425-25dupCA
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-26_2401-25dupCA
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-26_2326-25dupCA
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-26_2302-25dupCA
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-26_2425-25dupCA
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38659
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/19-50764711-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764711
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764711
    reference: chr 19
allele count: 1
allele frequency: 9.057478760212308e-6
allele num: 110406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-21C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-21C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-21C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-21C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-21C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-21C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-21C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-21C>A
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5874
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

19-50764714-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764714
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764713
    reference: chr 19
allele count: 1
allele frequency: 8.912814845184407e-6
allele num: 112198
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-17delT
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-17delT
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-17delT
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-17delT
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-17delT
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-17delT
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-17delT
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-17delT
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38070
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: CT
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

19-50764716-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764716
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764716
    reference: chr 19
allele count: 1
allele frequency: 8.850027435085049e-6
allele num: 112994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-16C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-16C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-16C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-16C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-16C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-16C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-16C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-16C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS

19-50764718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764718
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764718
    reference: chr 19
allele count: 2
allele frequency: 1.755802928679285e-5
allele num: 113908
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-14C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-14C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-14C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-14C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-14C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-14C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-14C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-14C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2911
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

19-50764721-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764721
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764721
    reference: chr 19
allele count: 1
allele frequency: 8.712622847982157e-6
allele num: 114776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-11A>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-11A>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-11A>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-11A>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-11A>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-11A>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-11A>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-11A>G
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38965
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/19-50764723-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764723
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764723
    reference: chr 19
allele count: 3
allele frequency: 2.597447574849781e-5
allele num: 115498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-9C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-9C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-9C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-9C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-9C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-9C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-9C>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-9C>A
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2225
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6312
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

19-50764724-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764724
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764724
    reference: chr 19
allele count: 3
allele frequency: 2.593047176171625e-5
allele num: 115694
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2326-8C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2425-8C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2425-8C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2302-8C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2425-8C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2326-8C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2401-8C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2326-8C>G
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.75e1
  variant carriers: 0
hgvs: c.2425-8C>G
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-50764738-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764738
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764738
    reference: chr 19
allele count: 2
allele frequency: 1.702359470225733e-5
allele num: 117484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2431G>C
  hgvsp: ENSP00000262269.8:p.Ala811Pro
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2431G>C
  hgvsp: ENSP00000470298.1:p.Ala811Pro
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2308G>C
  hgvsp: ENSP00000472819.1:p.Ala770Pro
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2407G>C
  hgvsp: ENSP00000366169.2:p.Ala803Pro
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2332G>C
  hgvsp: ENSP00000469573.1:p.Ala778Pro
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2431G>C
  hgvsp: ENSP00000406273.2:p.Ala811Pro
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2332G>C
  hgvsp: ENSP00000407879.1:p.Ala778Pro
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2332G>C
  hgvsp: ENSP00000472543.1:p.Ala778Pro
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala811Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

19-50764738-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764738
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764738
    reference: chr 19
allele count: 1
allele frequency: 8.511797351128664e-6
allele num: 117484
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2431G>T
  hgvsp: ENSP00000470298.1:p.Ala811Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2308G>T
  hgvsp: ENSP00000472819.1:p.Ala770Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2332G>T
  hgvsp: ENSP00000472543.1:p.Ala778Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2407G>T
  hgvsp: ENSP00000366169.2:p.Ala803Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2332G>T
  hgvsp: ENSP00000407879.1:p.Ala778Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2431G>T
  hgvsp: ENSP00000262269.8:p.Ala811Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2431G>T
  hgvsp: ENSP00000406273.2:p.Ala811Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2332G>T
  hgvsp: ENSP00000469573.1:p.Ala778Ser
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48216
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala811Ser
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

19-50764739-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764739
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764739
    reference: chr 19
allele count: 58
allele frequency: 4.934406424937469e-4
allele num: 117542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2408C>T
  hgvsp: ENSP00000366169.2:p.Ala803Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2432C>T
  hgvsp: ENSP00000406273.2:p.Ala811Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2333C>T
  hgvsp: ENSP00000407879.1:p.Ala778Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2333C>T
  hgvsp: ENSP00000472543.1:p.Ala778Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2432C>T
  hgvsp: ENSP00000262269.8:p.Ala811Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2432C>T
  hgvsp: ENSP00000470298.1:p.Ala811Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2333C>T
  hgvsp: ENSP00000469573.1:p.Ala778Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2309C>T
  hgvsp: ENSP00000472819.1:p.Ala770Val
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15089
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 39610
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48182
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala811Val
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-50764740-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764740
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764740
    reference: chr 19
allele count: 7
allele frequency: 5.950154704022305e-5
allele num: 117644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2409G>A
  hgvsp: ENST00000376970.2:c.2409G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2310G>A
  hgvsp: ENST00000596571.1:c.2310G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2433G>A
  hgvsp: ENST00000601313.1:c.2433G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2334G>A
  hgvsp: ENST00000599920.1:c.2334G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2433G>A
  hgvsp: ENST00000440075.2:c.2433G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2433G>A
  hgvsp: ENST00000262269.8:c.2433G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2334G>A
  hgvsp: ENST00000598205.1:c.2334G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2334G>A
  hgvsp: ENST00000425460.1:c.2334G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15146
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala811Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

19-50764740-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764740
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764740
    reference: chr 19
allele count: 1
allele frequency: 8.500221005746149e-6
allele num: 117644
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2334G>T
  hgvsp: ENST00000598205.1:c.2334G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2334G>T
  hgvsp: ENST00000425460.1:c.2334G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2310G>T
  hgvsp: ENST00000596571.1:c.2310G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2433G>T
  hgvsp: ENST00000440075.2:c.2433G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2409G>T
  hgvsp: ENST00000376970.2:c.2409G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2334G>T
  hgvsp: ENST00000599920.1:c.2334G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2433G>T
  hgvsp: ENST00000262269.8:c.2433G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2433G>T
  hgvsp: ENST00000601313.1:c.2433G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15146
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala811Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

19-50764741-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764741
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764741
    reference: chr 19
allele count: 2
allele frequency: 1.698802344347235e-5
allele num: 117730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2434C>T
  hgvsp: ENST00000440075.2:c.2434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2434C>T
  hgvsp: ENST00000262269.8:c.2434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2335C>T
  hgvsp: ENST00000598205.1:c.2335C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2434C>T
  hgvsp: ENST00000601313.1:c.2434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2311C>T
  hgvsp: ENST00000596571.1:c.2311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2410C>T
  hgvsp: ENST00000376970.2:c.2410C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2335C>T
  hgvsp: ENST00000599920.1:c.2335C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2335C>T
  hgvsp: ENST00000425460.1:c.2335C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15182
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu812Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

19-50764747-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764747
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764747
    reference: chr 19
allele count: 1
allele frequency: 8.471417437565653e-6
allele num: 118044
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2440C>G
  hgvsp: ENSP00000406273.2:p.Leu814Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2416C>G
  hgvsp: ENSP00000366169.2:p.Leu806Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2341C>G
  hgvsp: ENSP00000469573.1:p.Leu781Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2341C>G
  hgvsp: ENSP00000472543.1:p.Leu781Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2440C>G
  hgvsp: ENSP00000470298.1:p.Leu814Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2440C>G
  hgvsp: ENSP00000262269.8:p.Leu814Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2341C>G
  hgvsp: ENSP00000407879.1:p.Leu781Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2317C>G
  hgvsp: ENSP00000472819.1:p.Leu773Val
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu814Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

19-50764752-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764752
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764752
    reference: chr 19
allele count: 2
allele frequency: 1.692104639750922e-5
allele num: 118196
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2421C>T
  hgvsp: ENST00000376970.2:c.2421C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2445C>T
  hgvsp: ENST00000601313.1:c.2445C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2322C>T
  hgvsp: ENST00000596571.1:c.2322C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2346C>T
  hgvsp: ENST00000425460.1:c.2346C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2445C>T
  hgvsp: ENST00000262269.8:c.2445C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2445C>T
  hgvsp: ENST00000440075.2:c.2445C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2346C>T
  hgvsp: ENST00000599920.1:c.2346C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2346C>T
  hgvsp: ENST00000598205.1:c.2346C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp815Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

19-50764758-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764758
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764758
    reference: chr 19
allele count: 1
allele frequency: 8.456087537418188e-6
allele num: 118258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2451C>T
  hgvsp: ENST00000262269.8:c.2451C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2427C>T
  hgvsp: ENST00000376970.2:c.2427C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2352C>T
  hgvsp: ENST00000598205.1:c.2352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2352C>T
  hgvsp: ENST00000425460.1:c.2352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2451C>T
  hgvsp: ENST00000601313.1:c.2451C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2451C>T
  hgvsp: ENST00000440075.2:c.2451C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2328C>T
  hgvsp: ENST00000596571.1:c.2328C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2352C>T
  hgvsp: ENST00000599920.1:c.2352C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48414
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn817Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/19-50764763-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764763
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764763
    reference: chr 19
allele count: 1
allele frequency: 8.45851942076059e-6
allele num: 118224
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2357A>C
  hgvsp: ENSP00000469573.1:p.Tyr786Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2456A>C
  hgvsp: ENSP00000470298.1:p.Tyr819Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2357A>C
  hgvsp: ENSP00000407879.1:p.Tyr786Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2333A>C
  hgvsp: ENSP00000472819.1:p.Tyr778Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2456A>C
  hgvsp: ENSP00000406273.2:p.Tyr819Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2456A>C
  hgvsp: ENSP00000262269.8:p.Tyr819Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2357A>C
  hgvsp: ENSP00000472543.1:p.Tyr786Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2432A>C
  hgvsp: ENSP00000366169.2:p.Tyr811Ser
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6503
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Tyr819Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

19-50764765-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764765
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764765
    reference: chr 19
allele count: 6
allele frequency: 5.073480915255957e-5
allele num: 118262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2458C>T
  hgvsp: ENSP00000262269.8:p.Arg820Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2359C>T
  hgvsp: ENSP00000469573.1:p.Arg787Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2434C>T
  hgvsp: ENSP00000366169.2:p.Arg812Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2359C>T
  hgvsp: ENSP00000472543.1:p.Arg787Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2458C>T
  hgvsp: ENSP00000406273.2:p.Arg820Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2335C>T
  hgvsp: ENSP00000472819.1:p.Arg779Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2359C>T
  hgvsp: ENSP00000407879.1:p.Arg787Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2458C>T
  hgvsp: ENSP00000470298.1:p.Arg820Cys
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg820Cys
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-50764766-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764766
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764766
    reference: chr 19
allele count: 2
allele frequency: 1.691274713751755e-5
allele num: 118254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2360G>A
  hgvsp: ENSP00000472543.1:p.Arg787His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2459G>A
  hgvsp: ENSP00000262269.8:p.Arg820His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2360G>A
  hgvsp: ENSP00000407879.1:p.Arg787His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2459G>A
  hgvsp: ENSP00000470298.1:p.Arg820His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2360G>A
  hgvsp: ENSP00000469573.1:p.Arg787His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2336G>A
  hgvsp: ENSP00000472819.1:p.Arg779His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2459G>A
  hgvsp: ENSP00000406273.2:p.Arg820His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2435G>A
  hgvsp: ENSP00000366169.2:p.Arg812His
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg820His
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-50764767-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764767
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764767
    reference: chr 19
allele count: 2
allele frequency: 1.690874351126968e-5
allele num: 118282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2460C>T
  hgvsp: ENST00000262269.8:c.2460C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2361C>T
  hgvsp: ENST00000425460.1:c.2361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2337C>T
  hgvsp: ENST00000596571.1:c.2337C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2460C>T
  hgvsp: ENST00000601313.1:c.2460C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2436C>T
  hgvsp: ENST00000376970.2:c.2436C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2361C>T
  hgvsp: ENST00000599920.1:c.2361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2460C>T
  hgvsp: ENST00000440075.2:c.2460C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2361C>T
  hgvsp: ENST00000598205.1:c.2361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg820Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-50764768-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764768
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764768
    reference: chr 19
allele count: 2
allele frequency: 1.690788583795482e-5
allele num: 118288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2437G>A
  hgvsp: ENSP00000366169.2:p.Val813Met
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2461G>A
  hgvsp: ENSP00000406273.2:p.Val821Met
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2362G>A
  hgvsp: ENSP00000469573.1:p.Val788Met
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2362G>A
  hgvsp: ENSP00000407879.1:p.Val788Met
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2461G>A
  hgvsp: ENSP00000262269.8:p.Val821Met
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2461G>A
  hgvsp: ENSP00000470298.1:p.Val821Met
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2338G>A
  hgvsp: ENSP00000472819.1:p.Val780Met
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2362G>A
  hgvsp: ENSP00000472543.1:p.Val788Met
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val821Met
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

19-50764770-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764770
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764770
    reference: chr 19
allele count: 1
allele frequency: 8.452799567216662e-6
allele num: 118304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2364G>A
  hgvsp: ENST00000599920.1:c.2364G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2463G>A
  hgvsp: ENST00000440075.2:c.2463G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2439G>A
  hgvsp: ENST00000376970.2:c.2439G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2364G>A
  hgvsp: ENST00000598205.1:c.2364G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2340G>A
  hgvsp: ENST00000596571.1:c.2340G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2463G>A
  hgvsp: ENST00000601313.1:c.2463G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2463G>A
  hgvsp: ENST00000262269.8:c.2463G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2364G>A
  hgvsp: ENST00000425460.1:c.2364G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6497
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val821Val
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

19-50764777-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764777
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764777
    reference: chr 19
allele count: 1
allele frequency: 8.454085859695991e-6
allele num: 118286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2347A>G
  hgvsp: ENSP00000472819.1:p.Ser783Gly
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2470A>G
  hgvsp: ENSP00000470298.1:p.Ser824Gly
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2371A>G
  hgvsp: ENSP00000472543.1:p.Ser791Gly
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2446A>G
  hgvsp: ENSP00000366169.2:p.Ser816Gly
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2470A>G
  hgvsp: ENSP00000262269.8:p.Ser824Gly
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2371A>G
  hgvsp: ENSP00000469573.1:p.Ser791Gly
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2371A>G
  hgvsp: ENSP00000407879.1:p.Ser791Gly
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2470A>G
  hgvsp: ENSP00000406273.2:p.Ser824Gly
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6464
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47931
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser824Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

19-50764778-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764778
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764778
    reference: chr 19
allele count: 17
allele frequency: 1.437413332431427e-4
allele num: 118268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2471G>C
  hgvsp: ENSP00000406273.2:p.Ser824Thr
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2471G>C
  hgvsp: ENSP00000262269.8:p.Ser824Thr
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2372G>C
  hgvsp: ENSP00000407879.1:p.Ser791Thr
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2348G>C
  hgvsp: ENSP00000472819.1:p.Ser783Thr
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2447G>C
  hgvsp: ENSP00000366169.2:p.Ser816Thr
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2372G>C
  hgvsp: ENSP00000469573.1:p.Ser791Thr
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2471G>C
  hgvsp: ENSP00000470298.1:p.Ser824Thr
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2372G>C
  hgvsp: ENSP00000472543.1:p.Ser791Thr
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser824Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

19-50764788-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764788
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764788
    reference: chr 19
allele count: 1
allele frequency: 8.468547813420954e-6
allele num: 118084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2382C>T
  hgvsp: ENST00000425460.1:c.2382C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2481C>T
  hgvsp: ENST00000440075.2:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2382C>T
  hgvsp: ENST00000599920.1:c.2382C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2481C>T
  hgvsp: ENST00000601313.1:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2358C>T
  hgvsp: ENST00000596571.1:c.2358C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2481C>T
  hgvsp: ENST00000262269.8:c.2481C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2382C>T
  hgvsp: ENST00000598205.1:c.2382C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2457C>T
  hgvsp: ENST00000376970.2:c.2457C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe827Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/19-50764792-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764792
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764792
    reference: chr 19
allele count: 1
allele frequency: 8.4774499830451e-6
allele num: 117960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2362C>A
  hgvsp: ENST00000596571.1:c.2362C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2386C>A
  hgvsp: ENST00000425460.1:c.2386C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2386C>A
  hgvsp: ENST00000598205.1:c.2386C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2485C>A
  hgvsp: ENST00000440075.2:c.2485C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2386C>A
  hgvsp: ENST00000599920.1:c.2386C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2461C>A
  hgvsp: ENST00000376970.2:c.2461C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2485C>A
  hgvsp: ENST00000262269.8:c.2485C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2485C>A
  hgvsp: ENST00000601313.1:c.2485C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46445
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg829Arg
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

19-50764793-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764793
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764793
    reference: chr 19
allele count: 1
allele frequency: 8.479318941102651e-6
allele num: 117934
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2387G>A
  hgvsp: ENSP00000407879.1:p.Arg796Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2486G>A
  hgvsp: ENSP00000262269.8:p.Arg829Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2363G>A
  hgvsp: ENSP00000472819.1:p.Arg788Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2387G>A
  hgvsp: ENSP00000469573.1:p.Arg796Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2486G>A
  hgvsp: ENSP00000470298.1:p.Arg829Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2462G>A
  hgvsp: ENSP00000366169.2:p.Arg821Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2486G>A
  hgvsp: ENSP00000406273.2:p.Arg829Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2387G>A
  hgvsp: ENSP00000472543.1:p.Arg796Gln
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6368
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg829Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

19-50764794-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764794
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764794
    reference: chr 19
allele count: 2
allele frequency: 1.69580627109159e-5
allele num: 117938
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2388G>A
  hgvsp: ENST00000425460.1:c.2388G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2463G>A
  hgvsp: ENST00000376970.2:c.2463G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2487G>A
  hgvsp: ENST00000601313.1:c.2487G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2388G>A
  hgvsp: ENST00000598205.1:c.2388G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2487G>A
  hgvsp: ENST00000262269.8:c.2487G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2487G>A
  hgvsp: ENST00000440075.2:c.2487G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2364G>A
  hgvsp: ENST00000596571.1:c.2364G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2388G>A
  hgvsp: ENST00000599920.1:c.2388G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46685
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg829Arg
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/19-50764809-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764809
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764809
    reference: chr 19
allele count: 1
allele frequency: 8.508321138073035e-6
allele num: 117532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2403C>A
  hgvsp: ENST00000425460.1:c.2403C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2478C>A
  hgvsp: ENST00000376970.2:c.2478C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2403C>A
  hgvsp: ENST00000599920.1:c.2403C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2502C>A
  hgvsp: ENST00000262269.8:c.2502C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2403C>A
  hgvsp: ENST00000598205.1:c.2403C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2379C>A
  hgvsp: ENST00000596571.1:c.2379C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2502C>A
  hgvsp: ENST00000601313.1:c.2502C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2502C>A
  hgvsp: ENST00000440075.2:c.2502C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1908
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala834Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

19-50764812-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764812
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764812
    reference: chr 19
allele count: 16
allele frequency: 1.388623700335005e-4
allele num: 115222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2406G>T
  hgvsp: ENSP00000407879.1:p.Gln802His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2406G>T
  hgvsp: ENSP00000469573.1:p.Gln802His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2505G>T
  hgvsp: ENSP00000262269.8:p.Gln835His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2505G>T
  hgvsp: ENSP00000406273.2:p.Gln835His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2481G>T
  hgvsp: ENSP00000366169.2:p.Gln827His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2382G>T
  hgvsp: ENSP00000472819.1:p.Gln794His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2505G>T
  hgvsp: ENSP00000470298.1:p.Gln835His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2406G>T
  hgvsp: ENSP00000472543.1:p.Gln802His
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15764
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 33683
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 3.25e1
  variant carriers: 4
hgvs: p.Gln835His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

19-50764824-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764824
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764824
    reference: chr 19
allele count: 4
allele frequency: 3.419563321763811e-5
allele num: 116974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2418G>T
  hgvsp: ENSP00000407879.1:p.Glu806Asp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2493G>T
  hgvsp: ENSP00000366169.2:p.Glu831Asp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2418G>T
  hgvsp: ENSP00000472543.1:p.Glu806Asp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2517G>T
  hgvsp: ENSP00000262269.8:p.Glu839Asp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2394G>T
  hgvsp: ENSP00000472819.1:p.Glu798Asp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2517G>T
  hgvsp: ENSP00000406273.2:p.Glu839Asp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2517G>T
  hgvsp: ENSP00000470298.1:p.Glu839Asp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2418G>T
  hgvsp: ENSP00000469573.1:p.Glu806Asp
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34710
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu839Asp
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

19-50764826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764826
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764826
    reference: chr 19
allele count: 2
allele frequency: 1.711566768219628e-5
allele num: 116852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2495G>A
  hgvsp: ENSP00000366169.2:p.Arg832Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2396G>A
  hgvsp: ENSP00000472819.1:p.Arg799Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2519G>A
  hgvsp: ENSP00000262269.8:p.Arg840Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2420G>A
  hgvsp: ENSP00000407879.1:p.Arg807Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2519G>A
  hgvsp: ENSP00000470298.1:p.Arg840Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2420G>A
  hgvsp: ENSP00000472543.1:p.Arg807Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2420G>A
  hgvsp: ENSP00000469573.1:p.Arg807Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2519G>A
  hgvsp: ENSP00000406273.2:p.Arg840Gln
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34577
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45103
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg840Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/19-50764829-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50764829
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50764828
    reference: chr 19
allele count: 1
allele frequency: 8.563550105331666e-6
allele num: 116774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.2401delC
  hgvsp: ENSP00000472819.1:p.Leu801Ter
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000407879
  ensembl transcript: ENST00000425460
  gene symbol: MYH14
  hgvsc: ENST00000425460.1:c.2425delC
  hgvsp: ENSP00000407879.1:p.Leu809Ter
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.2524delC
  hgvsp: ENSP00000406273.2:p.Leu842Ter
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.2500delC
  hgvsp: ENSP00000366169.2:p.Leu834Ter
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.2524delC
  hgvsp: ENSP00000470298.1:p.Leu842Ter
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000469573
  ensembl transcript: ENST00000599920
  gene symbol: MYH14
  hgvsc: ENST00000599920.1:c.2425delC
  hgvsp: ENSP00000469573.1:p.Leu809Ter
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.2524delC
  hgvsp: ENSP00000262269.8:p.Leu842Ter
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.2425delC
  hgvsp: ENSP00000472543.1:p.Leu809Ter
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17097
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu842Ter
num of homozygotes: 0
reference allele: AC

GenotypeQuality
all individuals: 580
bin: 5.25e1
variant carriers: 11

GenotypeQuality
all individuals: 7034
bin: 2.25e1
variant carriers: 19

GenotypeQuality
all individuals: 467
bin: 5.75e1
variant carriers: 14

GenotypeQuality
all individuals: 691
bin: 7.25e1
variant carriers: 16

GenotypeQuality
all individuals: 1245
bin: 3.75e1
variant carriers: 15

GenotypeQuality
all individuals: 1352
bin: 6.25e1
variant carriers: 15

GenotypeQuality
all individuals: 640
bin: 4.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1967
bin: 3.25e1
variant carriers: 22

GenotypeQuality
all individuals: 8220
bin: 7.5e0
variant carriers: 21

GenotypeQuality
all individuals: 738
bin: 7.75e1
variant carriers: 19

GenotypeQuality
all individuals: 2171
bin: 2.75e1
variant carriers: 16

GenotypeQuality
all individuals: 21289
bin: 9.75e1
variant carriers: 1552

African
type: Population
allele count: 452
allele frequency: 7.545909849749582e-2
allele num: 5990
num of homozygotes: 4

Latino
type: Population
allele count: 84
allele frequency: 1.671974522292994e-2
allele num: 5024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 109
allele frequency: 2.674190382728165e-2
allele num: 4076
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 898
allele frequency: 2.055296164057493e-2
allele num: 43692
num of homozygotes: 3

Other
type: Population
allele count: 5
allele frequency: 8.474576271186441e-3
allele num: 590
num of homozygotes: 0

South Asian
type: Population
allele count: 54
allele frequency: 4.353434376007739e-3
allele num: 12404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5962
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

MQ
type: SiteQuality
SIO_000300: 6.057e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.25e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
SIO_000300: 1.634e1

DP
type: SiteQuality
SIO_000300: 1.456518e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

GenotypeQuality
all individuals: 2171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2432
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5440
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 738
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21289
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1967
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7034
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4076
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.677289500167729e-4
allele num: 5962
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5024
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.612383102225089e-4
allele num: 12404
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.669449081803005e-4
allele num: 5990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.577497024626934e-5
allele num: 43692
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

MQ
type: SiteQuality
SIO_000300: 6.057e1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.25e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

DP
type: SiteQuality
SIO_000300: 1.456518e6

QD
type: SiteQuality
SIO_000300: 1.634e1

GenotypeQuality
all individuals: 2432
bin: 1.25e1
variant carriers: 10

GenotypeQuality
all individuals: 721
bin: 4.25e1
variant carriers: 33

GenotypeQuality
all individuals: 467
bin: 5.75e1
variant carriers: 30

GenotypeQuality
all individuals: 8220
bin: 7.5e0
variant carriers: 4

GenotypeQuality
all individuals: 1245
bin: 3.75e1
variant carriers: 23

GenotypeQuality
all individuals: 1967
bin: 3.25e1
variant carriers: 22

GenotypeQuality
all individuals: 2171
bin: 2.75e1
variant carriers: 14

GenotypeQuality
all individuals: 580
bin: 5.25e1
variant carriers: 28

GenotypeQuality
all individuals: 640
bin: 4.75e1
variant carriers: 31

GenotypeQuality
all individuals: 609
bin: 8.75e1
variant carriers: 23

GenotypeQuality
all individuals: 800
bin: 6.75e1
variant carriers: 31

GenotypeQuality
all individuals: 691
bin: 7.25e1
variant carriers: 42

European (Finnish)
type: Population
allele count: 24
allele frequency: 5.888125613346418e-3
allele num: 4076
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.845018450184502e-3
allele num: 5962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 299
allele frequency: 6.843358051817267e-3
allele num: 43692
num of homozygotes: 0

Latino
type: Population
allele count: 23
allele frequency: 4.578025477707006e-3
allele num: 5024
num of homozygotes: 0

South Asian
type: Population
allele count: 46
allele frequency: 3.708481135117704e-3
allele num: 12404
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 5.084745762711864e-3
allele num: 590
num of homozygotes: 0

African
type: Population
allele count: 50
allele frequency: 8.347245409015025e-3
allele num: 5990
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

DP
type: SiteQuality
SIO_000300: 1.456518e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

QD
type: SiteQuality
SIO_000300: 1.634e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.25e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.057e1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.677289500167729e-4
allele num: 5962
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4076
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1

QD
type: SiteQuality
SIO_000300: 1.634e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.25e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQ
type: SiteQuality
SIO_000300: 6.057e1

DP
type: SiteQuality
SIO_000300: 1.456518e6

GenotypeQuality
all individuals: 2486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4893
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3394
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2897
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1170
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11947
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3969
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.523595619038005e-5
allele num: 39626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3372
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.546e0

MQ
type: SiteQuality
SIO_000300: 5.465e1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.11e-1

QD
type: SiteQuality
SIO_000300: 6.34e0

DP
type: SiteQuality
SIO_000300: 1.501716e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.57e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.75e-1

GenotypeQuality
all individuals: 2893
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3602
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6963
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3193
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5442
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.009016229212583e-5
allele num: 39928
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

DP
type: SiteQuality
SIO_000300: 1.497758e6

QD
type: SiteQuality
SIO_000300: 2.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.742e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.08e-2

GenotypeQuality
all individuals: 655
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4602
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 411
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 534
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3343
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 498
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 268
bin: 8.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2605
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 539
bin: 8.25e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 221
allele frequency: 5.534962933279904e-3
allele num: 39928
num of homozygotes: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 2.388827636898199e-3
allele num: 5442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 38
allele frequency: 1.113716295427902e-2
allele num: 3412
num of homozygotes: 1

Latino
type: Population
allele count: 5
allele frequency: 1.463700234192038e-3
allele num: 3416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.742e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.08e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.497758e6

MQRankSum
type: SiteQuality
SIO_000300: -8.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

QD
type: SiteQuality
SIO_000300: 2.68e0

GenotypeQuality
all individuals: 3602
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4602
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2893
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 539
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12116
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.009016229212583e-5
allele num: 39928
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.537318712415989e-4
allele num: 5654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3416
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.44e-1

QD
type: SiteQuality
SIO_000300: 2.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQ
type: SiteQuality
SIO_000300: 5.742e1

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

DP
type: SiteQuality
SIO_000300: 1.497758e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.08e-2

GenotypeQuality
all individuals: 1305
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3929
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6857
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 2975
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6162
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 1119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1853
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.848038439199535e-4
allele num: 37878
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 5.798221878623889e-4
allele num: 5174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3120
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.824484583105273e-4
allele num: 10962
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3214
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 9.394964299135663e-4
allele num: 5322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

DP
type: SiteQuality
SIO_000300: 1.496259e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.071e-1

FS
type: SiteQuality
SIO_000300: 9.320000000000001e-1

QD
type: SiteQuality
SIO_000300: 7.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 491
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10536
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1853
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1305
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6162
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37878
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.739466563587167e-3
allele num: 5174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5322
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.915708812260536e-3
allele num: 522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10962
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.496259e6

FS
type: SiteQuality
SIO_000300: 9.320000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.071e-1

QD
type: SiteQuality
SIO_000300: 7.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5322
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 9.320000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.071e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.496259e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

QD
type: SiteQuality
SIO_000300: 7.48e0

GenotypeQuality
all individuals: 409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4914
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1853
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 762
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.280109826284386e-5
allele num: 37878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10962
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

MQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

QD
type: SiteQuality
SIO_000300: 7.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 9.320000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.071e-1

DP
type: SiteQuality
SIO_000300: 1.496259e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

GenotypeQuality
all individuals: 3837
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3480
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2975
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3929
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1119
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6857
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6162
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3120
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.932740626207963e-4
allele num: 5174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.640054913142193e-5
allele num: 37878
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10962
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.071e-1

DP
type: SiteQuality
SIO_000300: 1.496259e6

FS
type: SiteQuality
SIO_000300: 9.320000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 7.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

GenotypeQuality
all individuals: 617
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 3055
bin: 2.75e1
variant carriers: 17

GenotypeQuality
all individuals: 1339
bin: 1.75e1
variant carriers: 20

GenotypeQuality
all individuals: 651
bin: 7.75e1
variant carriers: 18

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 19

GenotypeQuality
all individuals: 585
bin: 8.25e1
variant carriers: 16

GenotypeQuality
all individuals: 1098
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2981
bin: 3.75e1
variant carriers: 25

GenotypeQuality
all individuals: 1693
bin: 6.25e1
variant carriers: 30

GenotypeQuality
all individuals: 1053
bin: 6.75e1
variant carriers: 32

GenotypeQuality
all individuals: 1496
bin: 4.75e1
variant carriers: 30

GenotypeQuality
all individuals: 24944
bin: 9.75e1
variant carriers: 77

Latino
type: Population
allele count: 65
allele frequency: 7.844557084238474e-3
allele num: 8286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 19
allele frequency: 3.85395537525355e-3
allele num: 4930
num of homozygotes: 0

East Asian
type: Population
allele count: 20
allele frequency: 2.913752913752914e-3
allele num: 6864
num of homozygotes: 0

African
type: Population
allele count: 33
allele frequency: 4.708904109589041e-3
allele num: 7008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 219
allele frequency: 4.256559766763849e-3
allele num: 51450
num of homozygotes: 0

South Asian
type: Population
allele count: 42
allele frequency: 3.06435137895812e-3
allele num: 13706
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 4.213483146067416e-3
allele num: 712
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.373283e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

MQ
type: SiteQuality
SIO_000300: 6.112e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.352e-1

QD
type: SiteQuality
SIO_000300: 2.129e1

GenotypeQuality
all individuals: 1098
bin: 1.25e1
variant carriers: 523

GenotypeQuality
all individuals: 3055
bin: 2.75e1
variant carriers: 1231

GenotypeQuality
all individuals: 700
bin: 7.25e1
variant carriers: 409

GenotypeQuality
all individuals: 1905
bin: 4.25e1
variant carriers: 1281

GenotypeQuality
all individuals: 1496
bin: 4.75e1
variant carriers: 881

GenotypeQuality
all individuals: 1339
bin: 1.75e1
variant carriers: 691

GenotypeQuality
all individuals: 1693
bin: 6.25e1
variant carriers: 521

GenotypeQuality
all individuals: 4986
bin: 2.25e1
variant carriers: 1069

GenotypeQuality
all individuals: 851
bin: 5.75e1
variant carriers: 789

GenotypeQuality
all individuals: 24944
bin: 9.75e1
variant carriers: 23005

GenotypeQuality
all individuals: 1053
bin: 6.75e1
variant carriers: 554

GenotypeQuality
all individuals: 1081
bin: 5.25e1
variant carriers: 848

Latino
type: Population
allele count: 5506
allele frequency: 6.644943277818006e-1
allele num: 8286
num of homozygotes: 1815

Other
type: Population
allele count: 296
allele frequency: 4.157303370786517e-1
allele num: 712
num of homozygotes: 55

African
type: Population
allele count: 2979
allele frequency: 4.250856164383562e-1
allele num: 7008
num of homozygotes: 658

European (Finnish)
type: Population
allele count: 2389
allele frequency: 4.845841784989858e-1
allele num: 4930
num of homozygotes: 575

East Asian
type: Population
allele count: 2165
allele frequency: 3.154137529137529e-1
allele num: 6864
num of homozygotes: 305

South Asian
type: Population
allele count: 5042
allele frequency: 3.678680869692106e-1
allele num: 13706
num of homozygotes: 938

European (Non-Finnish)
type: Population
allele count: 21604
allele frequency: 4.199028182701652e-1
allele num: 51450
num of homozygotes: 4399

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.373283e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

QD
type: SiteQuality
SIO_000300: 2.129e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.352e-1

MQ
type: SiteQuality
SIO_000300: 6.112e1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 1098
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1905
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24944
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1693
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.943634596695821e-5
allele num: 51450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7008
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13706
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

DP
type: SiteQuality
SIO_000300: 1.373283e6

MQ
type: SiteQuality
SIO_000300: 6.112e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.352e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 2.129e1

GenotypeQuality
all individuals: 585
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24944
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 3055
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1693
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 4986
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1339
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 851
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.413709872073377e-4
allele num: 8286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.943634596695821e-4
allele num: 51450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7008
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.648037355902525e-4
allele num: 13706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4930
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.373283e6

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

QD
type: SiteQuality
SIO_000300: 2.129e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.352e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

MQ
type: SiteQuality
SIO_000300: 6.112e1

GenotypeQuality
all individuals: 585
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3501
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1905
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24944
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 617
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4986
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8286
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.296074711805048e-5
allele num: 13706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.853881278538813e-4
allele num: 7008
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.112e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

DP
type: SiteQuality
SIO_000300: 1.373283e6

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.129e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.352e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13706
num of homozygotes: 0

African
type: Population
allele count: 66
allele frequency: 9.417808219178082e-3
allele num: 7008
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.352e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

MQ
type: SiteQuality
SIO_000300: 6.112e1

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

DP
type: SiteQuality
SIO_000300: 1.373283e6

QD
type: SiteQuality
SIO_000300: 2.129e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

GenotypeQuality
all individuals: 284
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21542
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1828
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2438
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1280
num of homozygotes: 0

Latino
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: 3080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5408
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.470000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e-1

QD
type: SiteQuality
SIO_000300: 5.47e0

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 1.436e0

MQ
type: SiteQuality
SIO_000300: 5.48e1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.51e-1

DP
type: SiteQuality
SIO_000300: 1.483239e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

GenotypeQuality
all individuals: 2600
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 534
bin: 7.25e1
variant carriers: 14

GenotypeQuality
all individuals: 641
bin: 7.75e1
variant carriers: 13

GenotypeQuality
all individuals: 7263
bin: 3.25e1
variant carriers: 16

GenotypeQuality
all individuals: 5188
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 5193
bin: 2.5e0
variant carriers: 4

GenotypeQuality
all individuals: 1227
bin: 6.75e1
variant carriers: 15

GenotypeQuality
all individuals: 5780
bin: 9.75e1
variant carriers: 1397

GenotypeQuality
all individuals: 2337
bin: 4.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2655
bin: 1.75e1
variant carriers: 9

European (Non-Finnish)
type: Population
allele count: 552
allele frequency: 1.170036881597355e-2
allele num: 47178
num of homozygotes: 5

European (Finnish)
type: Population
allele count: 146
allele frequency: 2.953074433656958e-2
allele num: 4944
num of homozygotes: 10

African
type: Population
allele count: 260
allele frequency: 3.820158683514546e-2
allele num: 6806
num of homozygotes: 7

South Asian
type: Population
allele count: 281
allele frequency: 2.249439641370477e-2
allele num: 12492
num of homozygotes: 11

Latino
type: Population
allele count: 93
allele frequency: 1.220792859018115e-2
allele num: 7618
num of homozygotes: 3

East Asian
type: Population
allele count: 1
allele frequency: 1.577287066246057e-4
allele num: 6340
num of homozygotes: 0

Other
type: Population
allele count: 15
allele frequency: 2.329192546583851e-2
allele num: 644
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.386135e6

MQ
type: SiteQuality
SIO_000300: 5.649e1

FS
type: SiteQuality
SIO_000300: 1.218e0

MQRankSum
type: SiteQuality
SIO_000300: -1.381e0

QD
type: SiteQuality
SIO_000300: 3.26e0

VQSLOD
type: SiteQuality
SIO_000300: 6.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.62e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.75e-1

GenotypeQuality
all individuals: 987
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2032
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5188
bin: 2.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2399
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1227
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 641
bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2297
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 534
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 459
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 537
bin: 8.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.202049311559398e-4
allele num: 12492
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.967484844630972e-4
allele num: 47178
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 5.877167205406994e-4
allele num: 6806
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.552795031055901e-3
allele num: 644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4944
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

MQ
type: SiteQuality
SIO_000300: 5.649e1

FS
type: SiteQuality
SIO_000300: 1.218e0

DP
type: SiteQuality
SIO_000300: 1.386135e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.62e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.381e0

QD
type: SiteQuality
SIO_000300: 3.26e0

VQSLOD
type: SiteQuality
SIO_000300: 6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.75e-1

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

GenotypeQuality
all individuals: 987
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 7.5e0
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GenotypeQuality
all individuals: 459
bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 537
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GenotypeQuality
all individuals: 5780
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.005123278898494e-5
allele num: 12492
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47178
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.15e-1

FS
type: SiteQuality
SIO_000300: 1.218e0

MQRankSum
type: SiteQuality
SIO_000300: -1.381e0

MQ
type: SiteQuality
SIO_000300: 5.649e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.75e-1

DP
type: SiteQuality
SIO_000300: 1.386135e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

QD
type: SiteQuality
SIO_000300: 3.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.62e-2

GenotypeQuality
all individuals: 2165
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 553
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variant carriers: 2

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 8125
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 4

GenotypeQuality
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bin: 2.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5093
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 382
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7478
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.517450682852807e-4
allele num: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.63708568810142e-5
allele num: 13094
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.0230116265036e-5
allele num: 49714
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.404e0

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 4.635e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.81e-2

QD
type: SiteQuality
SIO_000300: 1.236e1

DP
type: SiteQuality
SIO_000300: 1.316695e6

GenotypeQuality
all individuals: 2752
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 553
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variant carriers: 0

GenotypeQuality
all individuals: 5745
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.461988304093567e-3
allele num: 684
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4686
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.63708568810142e-5
allele num: 13094
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.404e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.81e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

DP
type: SiteQuality
SIO_000300: 1.316695e6

FS
type: SiteQuality
SIO_000300: 4.635e0

QD
type: SiteQuality
SIO_000300: 1.236e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.69e-1

GenotypeQuality
all individuals: 1026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9801
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4840
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 630
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variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1692
bin: 5.25e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4686
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.034901365705615e-4
allele num: 6590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49714
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.635e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.404e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.81e-2

DP
type: SiteQuality
SIO_000300: 1.316695e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 1.236e1

GenotypeQuality
all individuals: 5465
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1743
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 544
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variant carriers: 3

GenotypeQuality
all individuals: 1680
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1704
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
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variant carriers: 2

GenotypeQuality
all individuals: 8365
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 777
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variant carriers: 1

GenotypeQuality
all individuals: 1955
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variant carriers: 1

GenotypeQuality
all individuals: 2757
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 412
bin: 8.75e1
variant carriers: 7

GenotypeQuality
all individuals: 10156
bin: 2.25e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 1.294330830960394e-4
allele num: 7726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6772
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.849002849002849e-3
allele num: 702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51234
num of homozygotes: 0

South Asian
type: Population
allele count: 260
allele frequency: 1.927925255820851e-2
allele num: 13486
num of homozygotes: 6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.66e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.68e-1

QD
type: SiteQuality
SIO_000300: 1.406e1

DP
type: SiteQuality
SIO_000300: 1.314228e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.258e0

GenotypeQuality
all individuals: 4351
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 6091
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6605
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 68
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GenotypeQuality
all individuals: 57
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.19e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 8.859999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -8.639e-1

MQ
type: SiteQuality
SIO_000300: 5.521e1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 6.17505e5

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4979
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4588
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GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 1112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2795
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3238
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2984
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.51222813825467e-5
allele num: 22162
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.33819e5

QD
type: SiteQuality
SIO_000300: 3.082e1

MQ
type: SiteQuality
SIO_000300: 5.553e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.59e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.486e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.01e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.01e-1

GenotypeQuality
all individuals: 3614
bin: 3.75e1
variant carriers: 4

GenotypeQuality
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bin: 1.75e1
variant carriers: 8

GenotypeQuality
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bin: 4.75e1
variant carriers: 13

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 486

GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
all individuals: 5925
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 201
bin: 8.25e1
variant carriers: 10

GenotypeQuality
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bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 6459
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1328
bin: 6.75e1
variant carriers: 6

Other
type: Population
allele count: 2
allele frequency: 5.208333333333333e-3
allele num: 384
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 6.506180871828237e-4
allele num: 6148
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 3.543586109142452e-3
allele num: 5644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 10
allele frequency: 3.148614609571789e-3
allele num: 3176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 478
allele frequency: 1.307654429063851e-2
allele num: 36554
num of homozygotes: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5008
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 2.612540192926045e-3
allele num: 4976
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.731e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.23e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.3e0

DP
type: SiteQuality
SIO_000300: 7.48544e5

GenotypeQuality
all individuals: 14398
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18391
bin: 2.25e1
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GenotypeQuality
all individuals: 2653
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GenotypeQuality
all individuals: 1238
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variant carriers: 0

GenotypeQuality
all individuals: 4950
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4730
bin: 3.25e1
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GenotypeQuality
all individuals: 1041
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variant carriers: 0

GenotypeQuality
all individuals: 1421
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variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.677289500167729e-4
allele num: 5962
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3934
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.946e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

FS
type: SiteQuality
SIO_000300: 3.388e0

MQ
type: SiteQuality
SIO_000300: 5.65e1

QD
type: SiteQuality
SIO_000300: 2.389e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

DP
type: SiteQuality
SIO_000300: 9.0772e5

GenotypeQuality
all individuals: 650
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 796
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3927
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4298
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.11595429538722e-5
allele num: 47260
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.863e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.562e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.22e-1

DP
type: SiteQuality
SIO_000300: 9.84178e5

QD
type: SiteQuality
SIO_000300: 1.769e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2990
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variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51752
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4854
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6716
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.06951871657754e-4
allele num: 9350
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.286e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.445e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

DP
type: SiteQuality
SIO_000300: 1.075385e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.32e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 750
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5024
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6918
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9570
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.771618625277162e-4
allele num: 7216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.895878360444394e-5
allele num: 52746
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.163e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

FS
type: SiteQuality
SIO_000300: 2.82e0

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

DP
type: SiteQuality
SIO_000300: 1.099239e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

GenotypeQuality
all individuals: 587
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
all individuals: 451
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variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.976906439684643e-5
allele num: 57332
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.278118609406953e-4
allele num: 7824
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5756
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7734
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.421e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

FS
type: SiteQuality
SIO_000300: 1.0888e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.59e-1

QD
type: SiteQuality
SIO_000300: 1.008e1

MQ
type: SiteQuality
SIO_000300: 5.92e1

DP
type: SiteQuality
SIO_000300: 1.203962e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

GenotypeQuality
all individuals: 592
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 82

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.450417500517563e-5
allele num: 57964
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.791708796764409e-4
allele num: 7912
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10558
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.939746111210442e-5
allele num: 11186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5576
num of homozygotes: 0

East Asian
type: Population
allele count: 79
allele frequency: 9.974747474747475e-3
allele num: 7920
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 1.112e1

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

DP
type: SiteQuality
SIO_000300: 1.229032e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 409
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GenotypeQuality
all individuals: 1221
bin: 3.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5986
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.529084471421346e-4
allele num: 11862
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.230314960629921e-4
allele num: 8128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.525630593978845e-4
allele num: 58992
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.799e0

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

DP
type: SiteQuality
SIO_000300: 1.246998e6

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQ
type: SiteQuality
SIO_000300: 5.903e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.82e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 409
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GenotypeQuality
all individuals: 495
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11862
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.695145104420938e-5
allele num: 58992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8038
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

DP
type: SiteQuality
SIO_000300: 1.246998e6

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

FS
type: SiteQuality
SIO_000300: 5.799e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.82e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.145475372279496e-4
allele num: 8730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61592
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13476
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.372e0

VQSLOD
type: SiteQuality
SIO_000300: 5.98e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.082e1

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.41e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.307434e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 177
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.128158844765343e-4
allele num: 8864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11228
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62326
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.327433e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.69e-1

FS
type: SiteQuality
SIO_000300: 9.627000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 8.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.61e-1

QD
type: SiteQuality
SIO_000300: 1.071e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.49e-1

MQ
type: SiteQuality
SIO_000300: 5.923e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8934
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.596424010217114e-5
allele num: 62640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.3369e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

VQSLOD
type: SiteQuality
SIO_000300: -1.938e0

QD
type: SiteQuality
SIO_000300: 1.567e1

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.181e0

MQ
type: SiteQuality
SIO_000300: 5.807e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

FS
type: SiteQuality
SIO_000300: 1.668e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6165
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.217786648924373e-4
allele num: 9018
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.149e0

MQ
type: SiteQuality
SIO_000300: 5.888e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 9.827e0

QD
type: SiteQuality
SIO_000300: 3.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.821e0

DP
type: SiteQuality
SIO_000300: 1.347637e6

GenotypeQuality
all individuals: 6209
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.579229967467863e-5
allele num: 63322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9098
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: 8364
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.359879e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.034e0

FS
type: SiteQuality
SIO_000300: 3.986e0

MQ
type: SiteQuality
SIO_000300: 5.662e1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

VQSLOD
type: SiteQuality
SIO_000300: -1.692e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 9.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.205e0

GenotypeQuality
all individuals: 480
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
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variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
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variant carriers: 0

GenotypeQuality
all individuals: 46921
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63630
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.579098067287044e-4
allele num: 8382
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.458e-1

DP
type: SiteQuality
SIO_000300: 1.366351e6

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.014e1

FS
type: SiteQuality
SIO_000300: 1.765e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.694e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 87
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47057
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6355
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 102
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
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GenotypeQuality
all individuals: 129
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GenotypeQuality
all individuals: 132
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variant carriers: 0

GenotypeQuality
all individuals: 90
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variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.75e1
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GenotypeQuality
all individuals: 1400
bin: 7.25e1
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GenotypeQuality
all individuals: 2127
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15632
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9182
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.639915522703273e-4
allele num: 11364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63712
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.18e-1

QD
type: SiteQuality
SIO_000300: 1.193e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

DP
type: SiteQuality
SIO_000300: 1.368963e6

MQ
type: SiteQuality
SIO_000300: 5.939e1

FS
type: SiteQuality
SIO_000300: 7.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.361e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1350
bin: 2.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 6476
bin: 6.75e1
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GenotypeQuality
all individuals: 159
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 125
bin: 2.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.09664633202242e-5
allele num: 64586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9396
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16140
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 7.48e0

FS
type: SiteQuality
SIO_000300: 5.793e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.055e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.941e-1

DP
type: SiteQuality
SIO_000300: 1.387853e6

GenotypeQuality
all individuals: 1350
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6476
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1419
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.741258741258741e-5
allele num: 11440
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16140
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.941e-1

FS
type: SiteQuality
SIO_000300: 5.793e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.055e0

DP
type: SiteQuality
SIO_000300: 1.387853e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.25e-1

QD
type: SiteQuality
SIO_000300: 7.48e0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 211
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variant carriers: 57

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 51
allele frequency: 5.423224159931943e-3
allele num: 9404
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.15473441108545e-3
allele num: 866
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.741258741258741e-5
allele num: 11440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16164
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.738740133106331e-5
allele num: 64610
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.612e0

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.42e-1

MQ
type: SiteQuality
SIO_000300: 5.907e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 1.390558e6

QD
type: SiteQuality
SIO_000300: 1.112e1

GenotypeQuality
all individuals: 48303
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 123
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 57
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GenotypeQuality
all individuals: 461
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GenotypeQuality
all individuals: 6478
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GenotypeQuality
all individuals: 1417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 9.75e1
variant carriers: 7

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.236093943139679e-4
allele num: 16180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.73203847462345e-5
allele num: 64666
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9420
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.893e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 1.390825e6

VQSLOD
type: SiteQuality
SIO_000300: -1.378e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

FS
type: SiteQuality
SIO_000300: 2.706e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-1

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6478
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.061571125265393e-4
allele num: 9420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

MQ
type: SiteQuality
SIO_000300: 5.893e1

VQSLOD
type: SiteQuality
SIO_000300: -1.378e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

DP
type: SiteQuality
SIO_000300: 1.390825e6

FS
type: SiteQuality
SIO_000300: 2.706e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 1168
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GenotypeQuality
all individuals: 131
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.235330450895614e-4
allele num: 16190
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.324e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

MQ
type: SiteQuality
SIO_000300: 5.884e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: -9.548e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 1.391025e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.56e-1

QD
type: SiteQuality
SIO_000300: 1.042e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 6506
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541497101985448e-5
allele num: 64872
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9476
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 2.898e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 5.905e1

QD
type: SiteQuality
SIO_000300: 9.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: -6.667e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.44e-1

DP
type: SiteQuality
SIO_000300: 1.394213e6

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

GenotypeQuality
all individuals: 22
bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 6495
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variant carriers: 0

GenotypeQuality
all individuals: 1423
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.078438615933998e-5
allele num: 64968
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9488
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: 16284
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 1.044e1

FS
type: SiteQuality
SIO_000300: 9.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.376e0

VQSLOD
type: SiteQuality
SIO_000300: -2.589e0

DP
type: SiteQuality
SIO_000300: 1.396149e6

MQ
type: SiteQuality
SIO_000300: 5.833e1

GenotypeQuality
all individuals: 127
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 448
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variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65022
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.463e0

MQRankSum
type: SiteQuality
SIO_000300: -1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.506e0

MQ
type: SiteQuality
SIO_000300: 5.888e1

VQSLOD
type: SiteQuality
SIO_000300: -2.237e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.243e1

DP
type: SiteQuality
SIO_000300: 1.396207e6

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 103
bin: 4.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.538272212650751e-5
allele num: 65008
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e0

MQ
type: SiteQuality
SIO_000300: 5.81e1

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

DP
type: SiteQuality
SIO_000300: 1.395935e6

VQSLOD
type: SiteQuality
SIO_000300: -2.837e0

QD
type: SiteQuality
SIO_000300: 1.225e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 26
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GenotypeQuality
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GenotypeQuality
all individuals: 134
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GenotypeQuality
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GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.226794611551947e-5
allele num: 65028
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

DP
type: SiteQuality
SIO_000300: 1.397052e6

QD
type: SiteQuality
SIO_000300: 9.27e0

MQ
type: SiteQuality
SIO_000300: 5.902e1

VQSLOD
type: SiteQuality
SIO_000300: -5.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 1142
bin: 7.75e1
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GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.105263157894737e-4
allele num: 9500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65026
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.107e0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

DP
type: SiteQuality
SIO_000300: 1.396642e6

QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1417
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6515
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48327
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537373551025428e-5
allele num: 65046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.712319219376198e-5
allele num: 11478
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

QD
type: SiteQuality
SIO_000300: 8.91e0

DP
type: SiteQuality
SIO_000300: 1.396867e6

VQSLOD
type: SiteQuality
SIO_000300: -2.296e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.49e0

FS
type: SiteQuality
SIO_000300: 8.553000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48215
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 150
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6508
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537137235612395e-5
allele num: 65056
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.150818058801821e-5
allele num: 16258
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 9.91e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

DP
type: SiteQuality
SIO_000300: 1.396713e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.94e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 9.72e-1

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

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1147
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.710801393728223e-5
allele num: 11480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9508
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.66e-1

QD
type: SiteQuality
SIO_000300: 2.62e0

FS
type: SiteQuality
SIO_000300: 2.815e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -3.024e0

DP
type: SiteQuality
SIO_000300: 1.396657e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.77e-1

MQ
type: SiteQuality
SIO_000300: 5.829e1

GenotypeQuality
all individuals: 390
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16234
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65082
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.436e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

DP
type: SiteQuality
SIO_000300: 1.394724e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

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

GenotypeQuality
all individuals: 6453
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47840
bin: 6.25e1
variant carriers: 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: 2
allele frequency: 3.031221582297666e-4
allele num: 6598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16234
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 2.305351489257062e-4
allele num: 65066
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.785e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.395159e6

QD
type: SiteQuality
SIO_000300: 9.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.93e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e-1

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6400
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46769
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.538745614574998e-5
allele num: 64988
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

QD
type: SiteQuality
SIO_000300: 1.086e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.281e0

DP
type: SiteQuality
SIO_000300: 1.38946e6

VQSLOD
type: SiteQuality
SIO_000300: 5.81e-1

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

GenotypeQuality
all individuals: 364
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
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GenotypeQuality
all individuals: 1396
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540167570231641e-5
allele num: 64928
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.777e1

QD
type: SiteQuality
SIO_000300: 4.75e0

VQSLOD
type: SiteQuality
SIO_000300: -6.766e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 1.389205e6

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

GenotypeQuality
all individuals: 435
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 360
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 8.75e1
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GenotypeQuality
all individuals: 1117
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.177415369409439e-5
allele num: 16188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64914
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9430
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.78e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.15e-1

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

FS
type: SiteQuality
SIO_000300: 2.465e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.388984e6

VQSLOD
type: SiteQuality
SIO_000300: -1.705e0

GenotypeQuality
all individuals: 360
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1494
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1396
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.121790791427965e-4
allele num: 9426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64922
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.792e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.282e0

FS
type: SiteQuality
SIO_000300: 1.413e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.71e-1

DP
type: SiteQuality
SIO_000300: 1.388152e6

VQSLOD
type: SiteQuality
SIO_000300: -1.34e0

QD
type: SiteQuality
SIO_000300: 1.381e1

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544830995489093e-5
allele num: 64732
num of homozygotes: 0

African
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: 854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.383251e6

QD
type: SiteQuality
SIO_000300: 1.098e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.799e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 9.436999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -5.397999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 4.25e1
variant carriers: 2

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.043382584093052e-4
allele num: 63620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.172588832487309e-4
allele num: 6304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9114
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11188
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.208313194780087e-4
allele num: 8276
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15874
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.92e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

FS
type: SiteQuality
SIO_000300: 6.0475e1

VQSLOD
type: SiteQuality
SIO_000300: -1.782e1

DP
type: SiteQuality
SIO_000300: 1.432833e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.554e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

QD
type: SiteQuality
SIO_000300: 5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

GenotypeQuality
all individuals: 47
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 647
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 4.323389537397319e-4
allele num: 9252
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16034
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64474
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.025e0

FS
type: SiteQuality
SIO_000300: 4.225e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.96e-1

DP
type: SiteQuality
SIO_000300: 1.377807e6

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.918e1

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17813383600377e-4
allele num: 8488
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55265037418874e-5
allele num: 64406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

FS
type: SiteQuality
SIO_000300: 4.273e0

DP
type: SiteQuality
SIO_000300: 1.376443e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

MQ
type: SiteQuality
SIO_000300: 5.85e1

QD
type: SiteQuality
SIO_000300: 1.202e1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.669e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1164
bin: 7.25e1
variant carriers: 0