19-50796927-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796927
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796927
    reference: chr 19
allele count: 29
allele frequency: 2.542610647401276e-4
allele num: 114056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.5452C>T
  hgvsp: ENSP00000406273.2:p.Arg1818Cys
  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.5452C>T
  hgvsp: ENSP00000262269.8:p.Arg1818Cys
  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.5329C>T
  hgvsp: ENSP00000472819.1:p.Arg1777Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2631C>T
  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.5428C>T
  hgvsp: ENSP00000366169.2:p.Arg1810Cys
  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.5353C>T
  hgvsp: ENSP00000407879.1:p.Arg1785Cys
  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.5452C>T
  hgvsp: ENSP00000470298.1:p.Arg1818Cys
  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.5353C>T
  hgvsp: ENSP00000472543.1:p.Arg1785Cys
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6177
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2386
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg1818Cys
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

19-50796928-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796928
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796928
    reference: chr 19
allele count: 1
allele frequency: 8.775470804008634e-6
allele num: 113954
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.5453G>A
  hgvsp: ENSP00000470298.1:p.Arg1818His
  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.5330G>A
  hgvsp: ENSP00000472819.1:p.Arg1777His
  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.5354G>A
  hgvsp: ENSP00000472543.1:p.Arg1785His
  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.5354G>A
  hgvsp: ENSP00000407879.1:p.Arg1785His
  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.5429G>A
  hgvsp: ENSP00000366169.2:p.Arg1810His
  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.5453G>A
  hgvsp: ENSP00000262269.8:p.Arg1818His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2632G>A
  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.5453G>A
  hgvsp: ENSP00000406273.2:p.Arg1818His
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6417
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3375
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg1818His
num of homozygotes: 0
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: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

19-50796928-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796928
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796928
    reference: chr 19
allele count: 2
allele frequency: 1.755094160801727e-5
allele num: 113954
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.5453G>T
  hgvsp: ENSP00000470298.1:p.Arg1818Leu
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2632G>T
  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.5330G>T
  hgvsp: ENSP00000472819.1:p.Arg1777Leu
  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.5354G>T
  hgvsp: ENSP00000472543.1:p.Arg1785Leu
  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.5429G>T
  hgvsp: ENSP00000366169.2:p.Arg1810Leu
  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.5453G>T
  hgvsp: ENSP00000406273.2:p.Arg1818Leu
  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.5453G>T
  hgvsp: ENSP00000262269.8:p.Arg1818Leu
  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.5354G>T
  hgvsp: ENSP00000407879.1:p.Arg1785Leu
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6417
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3375
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5045
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg1818Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

19-50796937-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796937
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796937
    reference: chr 19
allele count: 1
allele frequency: 8.837201081673412e-6
allele num: 113158
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.5462T>C
  hgvsp: ENSP00000470298.1:p.Leu1821Pro
  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.5363T>C
  hgvsp: ENSP00000472543.1:p.Leu1788Pro
  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.5462T>C
  hgvsp: ENSP00000262269.8:p.Leu1821Pro
  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.5339T>C
  hgvsp: ENSP00000472819.1:p.Leu1780Pro
  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.5462T>C
  hgvsp: ENSP00000406273.2:p.Leu1821Pro
  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.5363T>C
  hgvsp: ENSP00000407879.1:p.Leu1788Pro
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2641T>C
  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.5438T>C
  hgvsp: ENSP00000366169.2:p.Leu1813Pro
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36763
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2929
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2379
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu1821Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

19-50796938-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796938
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796938
    reference: chr 19
allele count: 1
allele frequency: 8.847521809141259e-6
allele num: 113026
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.5439C>T
  hgvsp: ENST00000376970.2:c.5439C>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.5463C>T
  hgvsp: ENST00000262269.8:c.5463C>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.5463C>T
  hgvsp: ENST00000601313.1:c.5463C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2642C>T
  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.5340C>T
  hgvsp: ENST00000596571.1:c.5340C>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.5463C>T
  hgvsp: ENST00000440075.2:c.5463C>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.5364C>T
  hgvsp: ENST00000598205.1:c.5364C>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.5364C>T
  hgvsp: ENST00000425460.1:c.5364C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5407
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6416
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu1821Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

19-50796941-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796941
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796941
    reference: chr 19
allele count: 415
allele frequency: 3.685612788632327e-3
allele num: 112600
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.5367G>A
  hgvsp: ENST00000598205.1:c.5367G>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.5343G>A
  hgvsp: ENST00000596571.1:c.5343G>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.5367G>A
  hgvsp: ENST00000425460.1:c.5367G>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.5466G>A
  hgvsp: ENST00000262269.8:c.5466G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2645G>A
  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.5466G>A
  hgvsp: ENST00000440075.2:c.5466G>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.5466G>A
  hgvsp: ENST00000601313.1:c.5466G>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.5442G>A
  hgvsp: ENST00000376970.2:c.5442G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 3.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6416
  bin: 4.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4562
  bin: 5.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 5.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 3.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 7.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 4575
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 7.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 6.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 2.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2332
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 1
hgvs: p.Leu1822Leu
num of homozygotes: 5
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

19-50796950-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796950
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796950
    reference: chr 19
allele count: 2
allele frequency: 1.789997494003508e-5
allele num: 111732
alternate allele: T
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.5370+6C>T
  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.5445+6C>T
  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.5469+6C>T
  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.5346+6C>T
  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.5370+6C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+6C>T
  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.5469+6C>T
  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.5469+6C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1778
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4454
  bin: 6.25e1
  variant carriers: 0
hgvs: c.5469+6C>T
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-50796951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796951
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796951
    reference: chr 19
allele count: 4
allele frequency: 3.579994988007017e-5
allele num: 111732
alternate allele: A
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.5370+7G>A
  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.5469+7G>A
  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.5346+7G>A
  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.5445+7G>A
  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.5469+7G>A
  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.5469+7G>A
  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.5370+7G>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+7G>A
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6201
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1819
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4492
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
hgvs: c.5469+7G>A
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

19-50796956-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796956
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796955
    reference: chr 19
allele count: 1
allele frequency: 8.958646885974342e-6
allele num: 111624
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.5445+13delG
  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.5370+13delG
  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.5469+13delG
  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.5469+13delG
  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.5346+13delG
  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.5469+13delG
  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.5370+13delG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+13delG
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6203
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5359
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36926
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4522
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1928
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: TG
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

19-50796960-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796960
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796960
    reference: chr 19
allele count: 83768
allele frequency: 7.496286220535858e-1
allele num: 111746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+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.5469+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.5469+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.5469+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.5445+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.5370+16C>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.5370+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.5346+16C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 3.75e1
  variant carriers: 3191
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 2.25e1
  variant carriers: 826
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 7.75e1
  variant carriers: 2644
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 7.5e0
  variant carriers: 2617
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 4.25e1
  variant carriers: 4080
genotype depth: GenotypeDepth
  all individuals: 4034
  bin: 6.75e1
  variant carriers: 4021
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 8.75e1
  variant carriers: 1564
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 1.25e1
  variant carriers: 917
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 3.25e1
  variant carriers: 2281
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 5.75e1
  variant carriers: 5008
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 2.5e0
  variant carriers: 715
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 5.25e1
  variant carriers: 5145
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.75e1
  variant carriers: 545
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 6.25e1
  variant carriers: 4573
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 2.75e1
  variant carriers: 1487
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 8.25e1
  variant carriers: 2132
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 4.75e1
  variant carriers: 4731
genotype depth: GenotypeDepth
  all individuals: 3952
  bin: 9.75e1
  variant carriers: 3947
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 9.25e1
  variant carriers: 1198
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 7.25e1
  variant carriers: 3250
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 7.25e1
  variant carriers: 258
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.25e1
  variant carriers: 240
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 1.75e1
  variant carriers: 939
genotype quality: GenotypeQuality
  all individuals: 48205
  bin: 9.75e1
  variant carriers: 47845
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 2.5e0
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.75e1
  variant carriers: 165
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 7.75e1
  variant carriers: 478
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 2.25e1
  variant carriers: 807
num of homozygotes: 32271
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

19-50796961-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796961
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796961
    reference: chr 19
allele count: 2
allele frequency: 1.80835096475524e-5
allele num: 110598
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.5346+17G>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.5469+17G>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.5370+17G>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.5445+17G>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+17G>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.5469+17G>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.5370+17G>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.5469+17G>A
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1786
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2604
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

19-50796962-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796962
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796962
    reference: chr 19
allele count: 2
allele frequency: 1.808547194039029e-5
allele num: 110586
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+18C>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.5445+18C>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.5346+18C>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.5370+18C>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.5469+18C>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.5469+18C>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.5370+18C>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.5469+18C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5956
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5499
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5427
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1781
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2627
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2886
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum

19-50796968-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796968
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796968
    reference: chr 19
allele count: 1
allele frequency: 9.052067492215222e-6
allele num: 110472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+24C>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.5469+24C>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.5445+24C>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.5469+24C>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.5346+24C>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.5469+24C>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.5370+24C>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.5370+24C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2978
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5681
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

19-50796971-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796971
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796971
    reference: chr 19
allele count: 1
allele frequency: 9.055182280819313e-6
allele num: 110434
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.5346+27G>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.5370+27G>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+27G>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.5445+27G>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.5469+27G>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.5370+27G>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.5469+27G>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.5469+27G>C
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6352
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5675
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2847
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1545
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

19-50796973-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796973
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796973
    reference: chr 19
allele count: 1
allele frequency: 9.058627436770781e-6
allele num: 110392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+29C>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.5469+29C>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.5469+29C>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.5445+29C>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.5469+29C>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.5370+29C>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.5370+29C>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.5346+29C>G
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2844
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

19-50796973-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796973
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796973
    reference: chr 19
allele count: 1
allele frequency: 9.058627436770781e-6
allele num: 110392
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.5445+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.5370+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.5370+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.5469+29C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+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.5469+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.5346+29C>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.5469+29C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2890
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2844
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD

19-50796980-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796980
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796980
    reference: chr 19
allele count: 10
allele frequency: 9.069965715529595e-5
allele num: 110254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.5469+36C>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.5370+36C>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.5469+36C>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.5445+36C>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.5469+36C>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.5346+36C>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.5370+36C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+36C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5919
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32751
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

19-50796981-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796981
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796981
    reference: chr 19
allele count: 1
allele frequency: 9.070623877510296e-6
allele num: 110246
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.5469+37C>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.5445+37C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+37C>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.5370+37C>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.5469+37C>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.5370+37C>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.5469+37C>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.5346+37C>G
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6407
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5496
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1194
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2951
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2835
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

19-50796982-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796982
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796982
    reference: chr 19
allele count: 1
allele frequency: 9.071611299599035e-6
allele num: 110234
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.5469+38C>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.5445+38C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+38C>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.5346+38C>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.5370+38C>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.5469+38C>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.5469+38C>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.5370+38C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2427
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6407
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2928
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1760
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3039
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-50796984-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796984
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796984
    reference: chr 19
allele count: 15
allele frequency: 1.361408604102378e-4
allele num: 110180
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.5469+40T>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.5469+40T>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.5469+40T>C
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+40T>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.5370+40T>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.5346+40T>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.5370+40T>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.5445+40T>C
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6408
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5902
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5493
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2874
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

19-50796990-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50796990
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50796990
    reference: chr 19
allele count: 13
allele frequency: 1.180744777475023e-4
allele num: 110100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.5469+46T>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.5346+46T>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.5469+46T>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.5370+46T>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.5370+46T>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.5445+46T>A
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2648+46T>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.5469+46T>A
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5900
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5491
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1670
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2767
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2691
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2688
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

19-50804871-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804871
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804871
    reference: chr 19
allele count: 1
allele frequency: 8.558126797206627e-6
allele num: 116848
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.5470-47C>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.5470-47C>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.5371-47C>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.5371-47C>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.5446-47C>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.5347-47C>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.5470-47C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2649-47C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26828
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4316
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6673
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

19-50804872-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804872
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804870
    reference: chr 19
allele count: 1
allele frequency: 8.554612647139337e-6
allele num: 116896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.5446-43_5446-42delCT
  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.5470-43_5470-42delCT
  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.5470-43_5470-42delCT
  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.5470-43_5470-42delCT
  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.5371-43_5371-42delCT
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2649-43_2649-42delCT
  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.5347-43_5347-42delCT
  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.5371-43_5371-42delCT
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15980
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1660
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4053
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: CCT
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

19-50804874-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804874
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804874
    reference: chr 19
allele count: 2
allele frequency: 1.706572008805912e-5
allele num: 117194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2649-44T>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.5371-44T>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.5470-44T>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.5347-44T>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.5446-44T>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.5371-44T>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.5470-44T>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.5470-44T>C
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16249
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 917
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1892
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30756
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3411
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6787
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

19-50804875-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804875
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804875
    reference: chr 19
allele count: 1
allele frequency: 8.536939336509074e-6
allele num: 117138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2649-43C>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.5470-43C>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.5371-43C>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.5446-43C>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.5470-43C>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.5470-43C>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.5347-43C>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.5371-43C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3048
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6790
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 5.75e1
  variant carriers: 0
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: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

19-50804875-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804875
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804873
    reference: chr 19
allele count: 1
allele frequency: 8.536939336509074e-6
allele num: 117138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.5347-42_5347-41delTG
  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.5470-42_5470-41delTG
  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.5446-42_5446-41delTG
  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.5470-42_5470-41delTG
  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.5470-42_5470-41delTG
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2649-42_2649-41delTG
  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.5371-42_5371-41delTG
  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.5371-42_5371-41delTG
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6790
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3048
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CTG
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

19-50804885-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804885
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804885
    reference: chr 19
allele count: 6
allele frequency: 5.099265705738374e-5
allele num: 117664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2649-33A>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.5347-33A>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.5371-33A>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.5446-33A>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.5371-33A>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.5470-33A>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.5470-33A>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.5470-33A>G
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17799
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25761
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1671
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2004
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

19-50804888-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804888
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804888
    reference: chr 19
allele count: 3
allele frequency: 2.543752543752544e-5
allele num: 117936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.5470-30A>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.5470-30A>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.5446-30A>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2649-30A>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.5470-30A>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.5371-30A>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.5347-30A>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.5371-30A>G
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6235
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1602
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7358
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40252
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

19-50804893-ATCCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804893
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804889
    reference: chr 19
allele count: 1
allele frequency: 8.45337120443633e-6
allele num: 118296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.5371-17_5371-14delTTCC
  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.5371-17_5371-14delTTCC
  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.5347-17_5347-14delTTCC
  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.5446-17_5446-14delTTCC
  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.5470-17_5470-14delTTCC
  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.5470-17_5470-14delTTCC
  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.5470-17_5470-14delTTCC
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2649-17_2649-14delTTCC
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7533
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: ATCCT
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

19-50804906-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804906
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804906
    reference: chr 19
allele count: 1
allele frequency: 8.382510729613734e-6
allele num: 119296
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.5371-12C>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.5470-12C>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.5446-12C>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.5371-12C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2649-12C>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.5470-12C>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.5470-12C>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.5347-12C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7863
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1906
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-50804908-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804908
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804908
    reference: chr 19
allele count: 2
allele frequency: 1.674452872523903e-5
allele num: 119442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.5470-10C>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.5371-10C>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.5470-10C>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.5371-10C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2649-10C>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.5446-10C>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.5347-10C>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.5470-10C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20145
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28616
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1903
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

19-50804921-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804921
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804921
    reference: chr 19
allele count: 1
allele frequency: 8.33541718763024e-6
allele num: 119970
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.5350G>C
  hgvsp: ENSP00000472819.1:p.Glu1784Gln
  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.5374G>C
  hgvsp: ENSP00000472543.1:p.Glu1792Gln
  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.5473G>C
  hgvsp: ENSP00000470298.1:p.Glu1825Gln
  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.5374G>C
  hgvsp: ENSP00000407879.1:p.Glu1792Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2652G>C
  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.5473G>C
  hgvsp: ENSP00000262269.8:p.Glu1825Gln
  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.5449G>C
  hgvsp: ENSP00000366169.2:p.Glu1817Gln
  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.5473G>C
  hgvsp: ENSP00000406273.2:p.Glu1825Gln
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu1825Gln
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

19-50804929-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804929
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804929
    reference: chr 19
allele count: 1
allele frequency: 8.323899580475461e-6
allele num: 120136
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.5358G>A
  hgvsp: ENST00000596571.1:c.5358G>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.5382G>A
  hgvsp: ENST00000598205.1:c.5382G>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.5481G>A
  hgvsp: ENST00000262269.8:c.5481G>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.5457G>A
  hgvsp: ENST00000376970.2:c.5457G>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.5382G>A
  hgvsp: ENST00000425460.1:c.5382G>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.5481G>A
  hgvsp: ENST00000601313.1:c.5481G>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.5481G>A
  hgvsp: ENST00000440075.2:c.5481G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2660G>A
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7096
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44827
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu1827Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

19-50804942-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804942
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804942
    reference: chr 19
allele count: 1
allele frequency: 8.312137383006666e-6
allele num: 120306
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.5494T>G
  hgvsp: ENSP00000470298.1:p.Ser1832Ala
  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.5395T>G
  hgvsp: ENSP00000407879.1:p.Ser1799Ala
  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.5494T>G
  hgvsp: ENSP00000262269.8:p.Ser1832Ala
  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.5371T>G
  hgvsp: ENSP00000472819.1:p.Ser1791Ala
  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.5470T>G
  hgvsp: ENSP00000366169.2:p.Ser1824Ala
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2673T>G
  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.5494T>G
  hgvsp: ENSP00000406273.2:p.Ser1832Ala
  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.5395T>G
  hgvsp: ENSP00000472543.1:p.Ser1799Ala
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44899
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser1832Ala
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum

19-50804951-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804951
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804951
    reference: chr 19
allele count: 2
allele frequency: 1.661819692563357e-5
allele num: 120350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.5380C>T
  hgvsp: ENSP00000472819.1:p.Arg1794Cys
  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.5404C>T
  hgvsp: ENSP00000407879.1:p.Arg1802Cys
  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.5503C>T
  hgvsp: ENSP00000262269.8:p.Arg1835Cys
  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.5503C>T
  hgvsp: ENSP00000470298.1:p.Arg1835Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2682C>T
  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.5479C>T
  hgvsp: ENSP00000366169.2:p.Arg1827Cys
  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.5404C>T
  hgvsp: ENSP00000472543.1:p.Arg1802Cys
  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.5503C>T
  hgvsp: ENSP00000406273.2:p.Arg1835Cys
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1818
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Arg1835Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

19-50804952-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804952
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804952
    reference: chr 19
allele count: 1
allele frequency: 8.308546170591069e-6
allele num: 120358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.5504G>A
  hgvsp: ENSP00000406273.2:p.Arg1835His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2683G>A
  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.5405G>A
  hgvsp: ENSP00000472543.1:p.Arg1802His
  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.5504G>A
  hgvsp: ENSP00000262269.8:p.Arg1835His
  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.5480G>A
  hgvsp: ENSP00000366169.2:p.Arg1827His
  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.5381G>A
  hgvsp: ENSP00000472819.1:p.Arg1794His
  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.5504G>A
  hgvsp: ENSP00000470298.1:p.Arg1835His
  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.5405G>A
  hgvsp: ENSP00000407879.1:p.Arg1802His
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21068
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1818
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg1835His
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-50804964-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804964
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804964
    reference: chr 19
allele count: 11
allele frequency: 9.138185987007161e-5
allele num: 120374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.5393C>A
  hgvsp: ENSP00000472819.1:p.Ala1798Asp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2695C>A
  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.5516C>A
  hgvsp: ENSP00000262269.8:p.Ala1839Asp
  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.5492C>A
  hgvsp: ENSP00000366169.2:p.Ala1831Asp
  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.5516C>A
  hgvsp: ENSP00000470298.1:p.Ala1839Asp
  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.5417C>A
  hgvsp: ENSP00000407879.1:p.Ala1806Asp
  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.5516C>A
  hgvsp: ENSP00000406273.2:p.Ala1839Asp
  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.5417C>A
  hgvsp: ENSP00000472543.1:p.Ala1806Asp
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala1839Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD

19-50804976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804976
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804976
    reference: chr 19
allele count: 1
allele frequency: 8.311170212765958e-6
allele num: 120320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000262269
  ensembl transcript: ENST00000262269
  gene symbol: MYH14
  hgvsc: ENST00000262269.8:c.5528G>A
  hgvsp: ENSP00000262269.8:p.Ser1843Asn
  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.5528G>A
  hgvsp: ENSP00000470298.1:p.Ser1843Asn
  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.5429G>A
  hgvsp: ENSP00000407879.1:p.Ser1810Asn
  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.5405G>A
  hgvsp: ENSP00000472819.1:p.Ser1802Asn
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2707G>A
  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.5504G>A
  hgvsp: ENSP00000366169.2:p.Ser1835Asn
  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.5528G>A
  hgvsp: ENSP00000406273.2:p.Ser1843Asn
  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.5429G>A
  hgvsp: ENSP00000472543.1:p.Ser1810Asn
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8153
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser1843Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

19-50804977-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804977
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804977
    reference: chr 19
allele count: 760
allele frequency: 6.316804361919643e-3
allele num: 120314
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.5529C>T
  hgvsp: ENST00000601313.1:c.5529C>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.5529C>T
  hgvsp: ENST00000440075.2:c.5529C>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.5529C>T
  hgvsp: ENST00000262269.8:c.5529C>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.5430C>T
  hgvsp: ENST00000425460.1:c.5430C>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.5406C>T
  hgvsp: ENST00000596571.1:c.5406C>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.5505C>T
  hgvsp: ENST00000376970.2:c.5505C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2708C>T
  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.5430C>T
  hgvsp: ENST00000598205.1:c.5430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27995
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21001
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 62
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 9.75e1
  variant carriers: 731
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1918
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser1843Ser
num of homozygotes: 26
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ

19-50804978-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804978
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804978
    reference: chr 19
allele count: 3
allele frequency: 2.493102416647276e-5
allele num: 120332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2709G>A
  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.5530G>A
  hgvsp: ENSP00000470298.1:p.Gly1844Arg
  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.5431G>A
  hgvsp: ENSP00000472543.1:p.Gly1811Arg
  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.5407G>A
  hgvsp: ENSP00000472819.1:p.Gly1803Arg
  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.5506G>A
  hgvsp: ENSP00000366169.2:p.Gly1836Arg
  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.5530G>A
  hgvsp: ENSP00000262269.8:p.Gly1844Arg
  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.5530G>A
  hgvsp: ENSP00000406273.2:p.Gly1844Arg
  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.5431G>A
  hgvsp: ENSP00000407879.1:p.Gly1811Arg
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21371
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly1844Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

19-50804981-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804981
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804981
    reference: chr 19
allele count: 175
allele frequency: 1.454720776737768e-3
allele num: 120298
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.5533C>T
  hgvsp: ENSP00000262269.8:p.Arg1845Trp
  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.5509C>T
  hgvsp: ENSP00000366169.2:p.Arg1837Trp
  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.5434C>T
  hgvsp: ENSP00000407879.1:p.Arg1812Trp
  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.5410C>T
  hgvsp: ENSP00000472819.1:p.Arg1804Trp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2712C>T
  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.5533C>T
  hgvsp: ENSP00000406273.2:p.Arg1845Trp
  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.5533C>T
  hgvsp: ENSP00000470298.1:p.Arg1845Trp
  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.5434C>T
  hgvsp: ENSP00000472543.1:p.Arg1812Trp
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 21342
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 5.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7300
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 44882
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 9.75e1
  variant carriers: 173
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg1845Trp
num of homozygotes: 2
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP

19-50804982-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804982
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804982
    reference: chr 19
allele count: 3
allele frequency: 2.494014365522746e-5
allele num: 120288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.5534G>A
  hgvsp: ENSP00000406273.2:p.Arg1845Gln
  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.5411G>A
  hgvsp: ENSP00000472819.1:p.Arg1804Gln
  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.5534G>A
  hgvsp: ENSP00000470298.1:p.Arg1845Gln
  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.5435G>A
  hgvsp: ENSP00000407879.1:p.Arg1812Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2713G>A
  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.5534G>A
  hgvsp: ENSP00000262269.8:p.Arg1845Gln
  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.5510G>A
  hgvsp: ENSP00000366169.2:p.Arg1837Gln
  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.5435G>A
  hgvsp: ENSP00000472543.1:p.Arg1812Gln
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7323
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44888
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1953
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg1845Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

19-50804990-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804990
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804990
    reference: chr 19
allele count: 1
allele frequency: 8.3166999334664e-6
allele num: 120240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000366169
  ensembl transcript: ENST00000376970
  gene symbol: MYH14
  hgvsc: ENST00000376970.2:c.5518C>G
  hgvsp: ENSP00000366169.2:p.Leu1840Val
  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.5443C>G
  hgvsp: ENSP00000407879.1:p.Leu1815Val
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2721C>G
  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.5443C>G
  hgvsp: ENSP00000472543.1:p.Leu1815Val
  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.5542C>G
  hgvsp: ENSP00000262269.8:p.Leu1848Val
  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.5419C>G
  hgvsp: ENSP00000472819.1:p.Leu1807Val
  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.5542C>G
  hgvsp: ENSP00000406273.2:p.Leu1848Val
  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.5542C>G
  hgvsp: ENSP00000470298.1:p.Leu1848Val
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 844
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu1848Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

19-50804992-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804992
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804992
    reference: chr 19
allele count: 1
allele frequency: 8.319467554076538e-6
allele num: 120200
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.5520G>A
  hgvsp: ENST00000376970.2:c.5520G>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.5544G>A
  hgvsp: ENST00000262269.8:c.5544G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2723G>A
  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.5445G>A
  hgvsp: ENST00000598205.1:c.5445G>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.5544G>A
  hgvsp: ENST00000440075.2:c.5544G>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.5544G>A
  hgvsp: ENST00000601313.1:c.5544G>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.5421G>A
  hgvsp: ENST00000596571.1:c.5421G>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.5445G>A
  hgvsp: ENST00000425460.1:c.5445G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21348
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1767
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu1848Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD

19-50804996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804996
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804996
    reference: chr 19
allele count: 3
allele frequency: 2.496878901373283e-5
allele num: 120150
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.5449C>T
  hgvsp: ENSP00000472543.1:p.Arg1817Trp
  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.5548C>T
  hgvsp: ENSP00000470298.1:p.Arg1850Trp
  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.5548C>T
  hgvsp: ENSP00000262269.8:p.Arg1850Trp
  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.5524C>T
  hgvsp: ENSP00000366169.2:p.Arg1842Trp
  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.5548C>T
  hgvsp: ENSP00000406273.2:p.Arg1850Trp
  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.5449C>T
  hgvsp: ENSP00000407879.1:p.Arg1817Trp
  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.5425C>T
  hgvsp: ENSP00000472819.1:p.Arg1809Trp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2727C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21329
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7334
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44588
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg1850Trp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

19-50804997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50804997
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50804997
    reference: chr 19
allele count: 3
allele frequency: 2.497585667188385e-5
allele num: 120116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2728G>A
  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.5549G>A
  hgvsp: ENSP00000406273.2:p.Arg1850Gln
  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.5525G>A
  hgvsp: ENSP00000366169.2:p.Arg1842Gln
  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.5450G>A
  hgvsp: ENSP00000407879.1:p.Arg1817Gln
  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.5450G>A
  hgvsp: ENSP00000472543.1:p.Arg1817Gln
  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.5549G>A
  hgvsp: ENSP00000262269.8:p.Arg1850Gln
  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.5549G>A
  hgvsp: ENSP00000470298.1:p.Arg1850Gln
  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.5426G>A
  hgvsp: ENSP00000472819.1:p.Arg1809Gln
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg1850Gln
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

19-50805001-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805001
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805001
    reference: chr 19
allele count: 1
allele frequency: 8.325424180361989e-6
allele num: 120114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.5553G>A
  hgvsp: ENST00000440075.2:c.5553G>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.5454G>A
  hgvsp: ENST00000598205.1:c.5454G>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.5454G>A
  hgvsp: ENST00000425460.1:c.5454G>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.5529G>A
  hgvsp: ENST00000376970.2:c.5529G>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.5430G>A
  hgvsp: ENST00000596571.1:c.5430G>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.5553G>A
  hgvsp: ENST00000262269.8:c.5553G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2732G>A
  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.5553G>A
  hgvsp: ENST00000601313.1:c.5553G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln1851Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-50805006-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805006
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805006
    reference: chr 19
allele count: 1
allele frequency: 8.331389342486753e-6
allele num: 120028
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2737A>C
  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.5558A>C
  hgvsp: ENSP00000470298.1:p.Gln1853Pro
  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.5459A>C
  hgvsp: ENSP00000407879.1:p.Gln1820Pro
  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.5558A>C
  hgvsp: ENSP00000262269.8:p.Gln1853Pro
  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.5459A>C
  hgvsp: ENSP00000472543.1:p.Gln1820Pro
  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.5534A>C
  hgvsp: ENSP00000366169.2:p.Gln1845Pro
  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.5435A>C
  hgvsp: ENSP00000472819.1:p.Gln1812Pro
  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.5558A>C
  hgvsp: ENSP00000406273.2:p.Gln1853Pro
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln1853Pro
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

19-50805014-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805014
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805014
    reference: chr 19
allele count: 7
allele frequency: 5.844632957050297e-5
allele num: 119768
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.5467C>T
  hgvsp: ENSP00000407879.1:p.Arg1823Trp
  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.5566C>T
  hgvsp: ENSP00000470298.1:p.Arg1856Trp
  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.5566C>T
  hgvsp: ENSP00000262269.8:p.Arg1856Trp
  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.5566C>T
  hgvsp: ENSP00000406273.2:p.Arg1856Trp
  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.5443C>T
  hgvsp: ENSP00000472819.1:p.Arg1815Trp
  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.5542C>T
  hgvsp: ENSP00000366169.2:p.Arg1848Trp
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2745C>T
  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.5467C>T
  hgvsp: ENSP00000472543.1:p.Arg1823Trp
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43516
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg1856Trp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

19-50805015-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805015
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805015
    reference: chr 19
allele count: 2
allele frequency: 1.671653767071764e-5
allele num: 119642
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.5468G>A
  hgvsp: ENSP00000407879.1:p.Arg1823Gln
  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.5567G>A
  hgvsp: ENSP00000262269.8:p.Arg1856Gln
  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.5543G>A
  hgvsp: ENSP00000366169.2:p.Arg1848Gln
  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.5468G>A
  hgvsp: ENSP00000472543.1:p.Arg1823Gln
  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.5567G>A
  hgvsp: ENSP00000406273.2:p.Arg1856Gln
  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.5567G>A
  hgvsp: ENSP00000470298.1:p.Arg1856Gln
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2746G>A
  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.5444G>A
  hgvsp: ENSP00000472819.1:p.Arg1815Gln
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7940
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg1856Gln
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

19-50805020-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805020
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805020
    reference: chr 19
allele count: 6
allele frequency: 5.017897166560734e-5
allele num: 119572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.5473C>T
  hgvsp: ENSP00000472543.1:p.Arg1825Cys
  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.5572C>T
  hgvsp: ENSP00000262269.8:p.Arg1858Cys
  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.5548C>T
  hgvsp: ENSP00000366169.2:p.Arg1850Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2751C>T
  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.5572C>T
  hgvsp: ENSP00000470298.1:p.Arg1858Cys
  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.5473C>T
  hgvsp: ENSP00000407879.1:p.Arg1825Cys
  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.5449C>T
  hgvsp: ENSP00000472819.1:p.Arg1817Cys
  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.5572C>T
  hgvsp: ENSP00000406273.2:p.Arg1858Cys
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42877
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1689
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1887
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg1858Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

19-50805021-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805021
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805021
    reference: chr 19
allele count: 62
allele frequency: 5.187937209224487e-4
allele num: 119508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.5450G>A
  hgvsp: ENSP00000472819.1:p.Arg1817His
  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.5549G>A
  hgvsp: ENSP00000366169.2:p.Arg1850His
  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.5573G>A
  hgvsp: ENSP00000470298.1:p.Arg1858His
  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.5474G>A
  hgvsp: ENSP00000407879.1:p.Arg1825His
  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.5573G>A
  hgvsp: ENSP00000406273.2:p.Arg1858His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2752G>A
  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.5573G>A
  hgvsp: ENSP00000262269.8:p.Arg1858His
  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.5474G>A
  hgvsp: ENSP00000472543.1:p.Arg1825His
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26315
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20813
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 8.25e1
  variant carriers: 1
hgvs: p.Arg1858His
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/19-50805022-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805022
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805022
    reference: chr 19
allele count: 1
allele frequency: 8.365960579593749e-6
allele num: 119532
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.5475C>A
  hgvsp: ENST00000425460.1:c.5475C>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.5475C>A
  hgvsp: ENST00000598205.1:c.5475C>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.5451C>A
  hgvsp: ENST00000596571.1:c.5451C>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.5550C>A
  hgvsp: ENST00000376970.2:c.5550C>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.5574C>A
  hgvsp: ENST00000601313.1:c.5574C>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.5574C>A
  hgvsp: ENST00000262269.8:c.5574C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2753C>A
  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.5574C>A
  hgvsp: ENST00000440075.2:c.5574C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20850
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1835
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg1858Arg
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

19-50805032-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805032
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805032
    reference: chr 19
allele count: 1
allele frequency: 8.413259296651523e-6
allele num: 118860
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.5584G>A
  hgvsp: ENSP00000470298.1:p.Glu1862Lys
  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.5485G>A
  hgvsp: ENSP00000472543.1:p.Glu1829Lys
  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.5584G>A
  hgvsp: ENSP00000262269.8:p.Glu1862Lys
  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.5584G>A
  hgvsp: ENSP00000406273.2:p.Glu1862Lys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2763G>A
  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.5485G>A
  hgvsp: ENSP00000407879.1:p.Glu1829Lys
  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.5461G>A
  hgvsp: ENSP00000472819.1:p.Glu1821Lys
  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.5560G>A
  hgvsp: ENSP00000366169.2:p.Glu1854Lys
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7019
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu1862Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

19-50805041-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805041
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805041
    reference: chr 19
allele count: 1
allele frequency: 8.496754239880366e-6
allele num: 117692
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.5494G>A
  hgvsp: ENSP00000472543.1:p.Gly1832Arg
  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.5494G>A
  hgvsp: ENSP00000407879.1:p.Gly1832Arg
  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.5470G>A
  hgvsp: ENSP00000472819.1:p.Gly1824Arg
  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.5593G>A
  hgvsp: ENSP00000406273.2:p.Gly1865Arg
  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.5593G>A
  hgvsp: ENSP00000262269.8:p.Gly1865Arg
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2772G>A
  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.5569G>A
  hgvsp: ENSP00000366169.2:p.Gly1857Arg
  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.5593G>A
  hgvsp: ENSP00000470298.1:p.Gly1865Arg
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6033
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly1865Arg
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

19-50805044-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805044
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805044
    reference: chr 19
allele count: 2
allele frequency: 1.739796095897561e-5
allele num: 114956
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.5572G>T
  hgvsp: ENSP00000366169.2:p.Ala1858Ser
  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.5596G>T
  hgvsp: ENSP00000470298.1:p.Ala1866Ser
  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.5473G>T
  hgvsp: ENSP00000472819.1:p.Ala1825Ser
  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.5497G>T
  hgvsp: ENSP00000407879.1:p.Ala1833Ser
  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.5497G>T
  hgvsp: ENSP00000472543.1:p.Ala1833Ser
  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.5596G>T
  hgvsp: ENSP00000262269.8:p.Ala1866Ser
  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.5596G>T
  hgvsp: ENSP00000406273.2:p.Ala1866Ser
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2775G>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23830
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3019
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1880
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27265
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala1866Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD

19-50805047-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805047
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805047
    reference: chr 19
allele count: 1
allele frequency: 8.677693122060432e-6
allele num: 115238
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.5599C>G
  hgvsp: ENSP00000470298.1:p.Arg1867Gly
  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.5500C>G
  hgvsp: ENSP00000472543.1:p.Arg1834Gly
  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.5500C>G
  hgvsp: ENSP00000407879.1:p.Arg1834Gly
  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.5476C>G
  hgvsp: ENSP00000472819.1:p.Arg1826Gly
  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.5599C>G
  hgvsp: ENSP00000262269.8:p.Arg1867Gly
  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.5575C>G
  hgvsp: ENSP00000366169.2:p.Arg1859Gly
  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.5599C>G
  hgvsp: ENSP00000406273.2:p.Arg1867Gly
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2778C>G
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3029
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg1867Gly
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-50805047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805047
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805047
    reference: chr 19
allele count: 17
allele frequency: 1.475207830750273e-4
allele num: 115238
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.5599C>T
  hgvsp: ENSP00000262269.8:p.Arg1867Cys
  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.5575C>T
  hgvsp: ENSP00000366169.2:p.Arg1859Cys
  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.5599C>T
  hgvsp: ENSP00000470298.1:p.Arg1867Cys
  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.5599C>T
  hgvsp: ENSP00000406273.2:p.Arg1867Cys
  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.5476C>T
  hgvsp: ENSP00000472819.1:p.Arg1826Cys
  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.5500C>T
  hgvsp: ENSP00000407879.1:p.Arg1834Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2778C>T
  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.5500C>T
  hgvsp: ENSP00000472543.1:p.Arg1834Cys
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23954
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6232
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18081
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4422
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2973
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29026
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg1867Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

19-50805048-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805048
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805048
    reference: chr 19
allele count: 1
allele frequency: 8.709132396230688e-6
allele num: 114822
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.5600G>A
  hgvsp: ENSP00000406273.2:p.Arg1867His
  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.5576G>A
  hgvsp: ENSP00000366169.2:p.Arg1859His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2779G>A
  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.5600G>A
  hgvsp: ENSP00000470298.1:p.Arg1867His
  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.5501G>A
  hgvsp: ENSP00000407879.1:p.Arg1834His
  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.5477G>A
  hgvsp: ENSP00000472819.1:p.Arg1826His
  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.5600G>A
  hgvsp: ENSP00000262269.8:p.Arg1867His
  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.5501G>A
  hgvsp: ENSP00000472543.1:p.Arg1834His
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23936
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2982
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2080
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3038
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg1867His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

19-50805050-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805050
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805050
    reference: chr 19
allele count: 1
allele frequency: 8.893948557401545e-6
allele num: 112436
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.5503G>C
  hgvsp: ENSP00000472543.1:p.Ala1835Pro
  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.5479G>C
  hgvsp: ENSP00000472819.1:p.Ala1827Pro
  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.5503G>C
  hgvsp: ENSP00000407879.1:p.Ala1835Pro
  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.5578G>C
  hgvsp: ENSP00000366169.2:p.Ala1860Pro
  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.5602G>C
  hgvsp: ENSP00000262269.8:p.Ala1868Pro
  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.5602G>C
  hgvsp: ENSP00000470298.1:p.Ala1868Pro
  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.5602G>C
  hgvsp: ENSP00000406273.2:p.Ala1868Pro
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2781G>C
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6234
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4392
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1998
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26925
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3054
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1527
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala1868Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

19-50805053-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805053
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805053
    reference: chr 19
allele count: 5
allele frequency: 4.249099190971514e-5
allele num: 117672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.5482C>T
  hgvsp: ENSP00000472819.1:p.Arg1828Cys
  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.5506C>T
  hgvsp: ENSP00000472543.1:p.Arg1836Cys
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2784C>T
  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.5605C>T
  hgvsp: ENSP00000262269.8:p.Arg1869Cys
  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.5581C>T
  hgvsp: ENSP00000366169.2:p.Arg1861Cys
  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.5506C>T
  hgvsp: ENSP00000407879.1:p.Arg1836Cys
  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.5605C>T
  hgvsp: ENSP00000470298.1:p.Arg1869Cys
  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.5605C>T
  hgvsp: ENSP00000406273.2:p.Arg1869Cys
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg1869Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

19-50805054-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805054
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805054
    reference: chr 19
allele count: 2
allele frequency: 1.701924877035928e-5
allele num: 117514
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472819
  ensembl transcript: ENST00000596571
  gene symbol: MYH14
  hgvsc: ENST00000596571.1:c.5483G>A
  hgvsp: ENSP00000472819.1:p.Arg1828His
  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.5507G>A
  hgvsp: ENSP00000472543.1:p.Arg1836His
  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.5606G>A
  hgvsp: ENSP00000406273.2:p.Arg1869His
  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.5606G>A
  hgvsp: ENSP00000470298.1:p.Arg1869His
  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.5582G>A
  hgvsp: ENSP00000366169.2:p.Arg1861His
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2785G>A
  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.5606G>A
  hgvsp: ENSP00000262269.8:p.Arg1869His
  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.5507G>A
  hgvsp: ENSP00000407879.1:p.Arg1836His
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41620
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg1869His
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

19-50805060-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805060
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805060
    reference: chr 19
allele count: 1
allele frequency: 8.520209937972871e-6
allele num: 117368
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.5489A>G
  hgvsp: ENSP00000472819.1:p.Lys1830Arg
  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.5612A>G
  hgvsp: ENSP00000262269.8:p.Lys1871Arg
  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.5612A>G
  hgvsp: ENSP00000406273.2:p.Lys1871Arg
  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.5513A>G
  hgvsp: ENSP00000407879.1:p.Lys1838Arg
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2791A>G
  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.5588A>G
  hgvsp: ENSP00000366169.2:p.Lys1863Arg
  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.5513A>G
  hgvsp: ENSP00000472543.1:p.Lys1838Arg
  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.5612A>G
  hgvsp: ENSP00000470298.1:p.Lys1871Arg
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys1871Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

19-50805062-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805062
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805062
    reference: chr 19
allele count: 1
allele frequency: 8.538251366120219e-6
allele num: 117120
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.5614A>T
  hgvsp: ENSP00000406273.2:p.Met1872Leu
  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.5614A>T
  hgvsp: ENSP00000470298.1:p.Met1872Leu
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2793A>T
  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.5614A>T
  hgvsp: ENSP00000262269.8:p.Met1872Leu
  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.5491A>T
  hgvsp: ENSP00000472819.1:p.Met1831Leu
  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.5515A>T
  hgvsp: ENSP00000472543.1:p.Met1839Leu
  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.5515A>T
  hgvsp: ENSP00000407879.1:p.Met1839Leu
  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.5590A>T
  hgvsp: ENSP00000366169.2:p.Met1864Leu
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23852
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42222
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met1872Leu
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

19-50805071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805071
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805071
    reference: chr 19
allele count: 2
allele frequency: 1.721852024037054e-5
allele num: 116154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2802G>A
  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.5524G>A
  hgvsp: ENSP00000407879.1:p.Ala1842Thr
  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.5599G>A
  hgvsp: ENSP00000366169.2:p.Ala1867Thr
  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.5623G>A
  hgvsp: ENSP00000406273.2:p.Ala1875Thr
  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.5623G>A
  hgvsp: ENSP00000262269.8:p.Ala1875Thr
  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.5623G>A
  hgvsp: ENSP00000470298.1:p.Ala1875Thr
  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.5500G>A
  hgvsp: ENSP00000472819.1:p.Ala1834Thr
  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.5524G>A
  hgvsp: ENSP00000472543.1:p.Ala1842Thr
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23290
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3679
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4477
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala1875Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

19-50805082-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805082
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805082
    reference: chr 19
allele count: 1
allele frequency: 8.762859496310836e-6
allele num: 114118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2813G>A
  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.5610G>A
  hgvsp: ENST00000376970.2:c.5610G>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.5634G>A
  hgvsp: ENST00000262269.8:c.5634G>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.5511G>A
  hgvsp: ENST00000596571.1:c.5511G>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.5634G>A
  hgvsp: ENST00000440075.2:c.5634G>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.5535G>A
  hgvsp: ENST00000598205.1:c.5535G>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.5634G>A
  hgvsp: ENST00000601313.1:c.5634G>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.5535G>A
  hgvsp: ENST00000425460.1:c.5535G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36726
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1552
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu1878Glu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

19-50805092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805092
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805092
    reference: chr 19
allele count: 3
allele frequency: 2.673082063619353e-5
allele num: 112230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000406273
  ensembl transcript: ENST00000440075
  gene symbol: MYH14
  hgvsc: ENST00000440075.2:c.5644G>A
  hgvsp: ENSP00000406273.2:p.Ala1882Thr
  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.5545G>A
  hgvsp: ENSP00000472543.1:p.Ala1849Thr
  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.5644G>A
  hgvsp: ENSP00000262269.8:p.Ala1882Thr
  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.5521G>A
  hgvsp: ENSP00000472819.1:p.Ala1841Thr
  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.5620G>A
  hgvsp: ENSP00000366169.2:p.Ala1874Thr
  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.5644G>A
  hgvsp: ENSP00000470298.1:p.Ala1882Thr
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2823G>A
  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.5545G>A
  hgvsp: ENSP00000407879.1:p.Ala1849Thr
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18719
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10357
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10030
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1217
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala1882Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/19-50805105-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805105
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805105
    reference: chr 19
allele count: 1
allele frequency: 9.107136352045463e-6
allele num: 109804
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000470298
  ensembl transcript: ENST00000601313
  gene symbol: MYH14
  hgvsc: ENST00000601313.1:c.5657A>C
  hgvsp: ENSP00000470298.1:p.Glu1886Ala
  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.5558A>C
  hgvsp: ENSP00000407879.1:p.Glu1853Ala
  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.5657A>C
  hgvsp: ENSP00000262269.8:p.Glu1886Ala
  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.5633A>C
  hgvsp: ENSP00000366169.2:p.Glu1878Ala
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2836A>C
  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.5657A>C
  hgvsp: ENSP00000406273.2:p.Glu1886Ala
  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.5534A>C
  hgvsp: ENSP00000472819.1:p.Glu1845Ala
  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.5558A>C
  hgvsp: ENSP00000472543.1:p.Glu1853Ala
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7109
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4851
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5638
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu1886Ala
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

19-50805121-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805121
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805121
    reference: chr 19
allele count: 1
allele frequency: 9.35401193571923e-6
allele num: 106906
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.5550G>A
  hgvsp: ENST00000596571.1:c.5550G>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.5673G>A
  hgvsp: ENST00000440075.2:c.5673G>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.5574G>A
  hgvsp: ENST00000598205.1:c.5574G>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.5574G>A
  hgvsp: ENST00000425460.1:c.5574G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2852G>A
  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.5649G>A
  hgvsp: ENST00000376970.2:c.5649G>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.5673G>A
  hgvsp: ENST00000262269.8:c.5673G>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.5673G>A
  hgvsp: ENST00000601313.1:c.5673G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9943
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14534
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13901
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu1891Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-50805138-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805138
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805138
    reference: chr 19
allele count: 1
allele frequency: 9.873812674025949e-6
allele num: 101278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl protein: ENSP00000472543
  ensembl transcript: ENST00000598205
  gene symbol: MYH14
  hgvsc: ENST00000598205.1:c.5579+12C>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.5555+12C>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.5654+12C>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.5678+12C>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.5579+12C>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.5678+12C>G
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2857+12C>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.5678+12C>G
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14478
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19056
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4565
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1040
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3978
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2774
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

19-50805138-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50805138
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 50805138
    reference: chr 19
allele count: 84063
allele frequency: 8.300223148166433e-1
allele num: 101278
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.5678+12C>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.5678+12C>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.5579+12C>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.5555+12C>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.5678+12C>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.5654+12C>T
  variant of: http://identifiers.org/hgnc/23212
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000105357
  ensembl transcript: ENST00000595016
  gene symbol: MYH14
  hgvsc: ENST00000595016.1:n.2857+12C>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.5579+12C>T
  variant of: http://identifiers.org/hgnc/23212
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7595
  bin: 2.25e1
  variant carriers: 7319
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 3.75e1
  variant carriers: 1256
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.75e1
  variant carriers: 821
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 7990
  bin: 7.5e0
  variant carriers: 7069
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 4.75e1
  variant carriers: 1130
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 387
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.25e1
  variant carriers: 1180
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 6.25e1
  variant carriers: 563
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 14478
  bin: 1.75e1
  variant carriers: 14281
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 2.75e1
  variant carriers: 3158
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 2.5e0
  variant carriers: 495
genotype depth: GenotypeDepth
  all individuals: 17471
  bin: 1.25e1
  variant carriers: 16568
num of homozygotes: 34792
reference allele: C

GenotypeQuality
all individuals: 36761
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 288
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5078
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3375
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1498
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 19
allele frequency: 2.206223873664654e-3
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.994404476418865e-4
allele num: 10008
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.575991756826378e-4
allele num: 11646
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64828
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.8e-2

DP
type: SiteQuality
SIO_000300: 2.668067e6

FS
type: SiteQuality
SIO_000300: 2.446e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 3.328e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

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

GenotypeQuality
all individuals: 247
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2385
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2415
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36755
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5045
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2223
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543162248078763e-5
allele num: 64802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.618e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 2.667484e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.67e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.26e-1

GenotypeQuality
all individuals: 1508
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36755
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2223
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2415
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2385
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10010
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.618e0

DP
type: SiteQuality
SIO_000300: 2.667484e6

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

GenotypeQuality
all individuals: 358
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1535
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4892
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11006
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.54765221159501e-5
allele num: 64614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9996
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.446e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.304e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

QD
type: SiteQuality
SIO_000300: 1.601e1

DP
type: SiteQuality
SIO_000300: 2.661843e6

GenotypeQuality
all individuals: 36766
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2237
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4891
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1507
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548467017652524e-5
allele num: 64580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10922
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.001e0

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.34e-1

FS
type: SiteQuality
SIO_000300: 4.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 2.66143e6

QD
type: SiteQuality
SIO_000300: 1.318e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1501
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 89
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 2.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 1718
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 535
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 228
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37044
bin: 9.75e1
variant carriers: 408

GenotypeQuality
all individuals: 4708
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 15
allele frequency: 1.304121022430882e-3
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.101352189554646e-5
allele num: 64488
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.326122354035822e-4
allele num: 8598
num of homozygotes: 0

South Asian
type: Population
allele count: 50
allele frequency: 4.71342383107089e-3
allele num: 10608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

African
type: Population
allele count: 346
allele frequency: 3.466239230615107e-2
allele num: 9982
num of homozygotes: 5

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.121e0

DP
type: SiteQuality
SIO_000300: 2.667696e6

FS
type: SiteQuality
SIO_000300: 5.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.16e1

GenotypeQuality
all individuals: 36924
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1899
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64314
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.992825827022718e-4
allele num: 10036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.661731e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.371e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 9.15e0

VQSLOD
type: SiteQuality
SIO_000300: 4.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

FS
type: SiteQuality
SIO_000300: 5.679999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1497
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2405
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36926
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1513
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.992825827022718e-4
allele num: 10036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.109839532280134e-5
allele num: 64312
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.661557e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.204e1

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

FS
type: SiteQuality
SIO_000300: 4.17e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.096e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.26e-1

GenotypeQuality
all individuals: 733
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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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bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
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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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bin: 6.75e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2335
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9894
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555645437291932e-5
allele num: 64282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.442e1

VQSLOD
type: SiteQuality
SIO_000300: 5.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.684e0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.661224e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

GenotypeQuality
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bin: 2.75e1
variant carriers: 271

GenotypeQuality
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variant carriers: 398

GenotypeQuality
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variant carriers: 628

GenotypeQuality
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GenotypeQuality
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variant carriers: 313

GenotypeQuality
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variant carriers: 238

GenotypeQuality
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variant carriers: 402

GenotypeQuality
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variant carriers: 128

GenotypeQuality
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variant carriers: 360

GenotypeQuality
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bin: 8.25e1
variant carriers: 627

GenotypeQuality
all individuals: 235
bin: 3.75e1
variant carriers: 206

GenotypeQuality
all individuals: 886
bin: 6.75e1
variant carriers: 293

European (Finnish)
type: Population
allele count: 5103
allele frequency: 7.724795640326976e-1
allele num: 6606
num of homozygotes: 1982

Other
type: Population
allele count: 618
allele frequency: 7.744360902255639e-1
allele num: 798
num of homozygotes: 237

African
type: Population
allele count: 3886
allele frequency: 3.938779647273464e-1
allele num: 9866
num of homozygotes: 782

East Asian
type: Population
allele count: 7993
allele frequency: 9.320195895522388e-1
allele num: 8576
num of homozygotes: 3729

South Asian
type: Population
allele count: 7919
allele frequency: 7.845254606697047e-1
allele num: 10094
num of homozygotes: 3105

Latino
type: Population
allele count: 10101
allele frequency: 8.794184224273028e-1
allele num: 11486
num of homozygotes: 4442

European (Non-Finnish)
type: Population
allele count: 48148
allele frequency: 7.485696517412935e-1
allele num: 64320
num of homozygotes: 17994

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

DP
type: SiteQuality
SIO_000300: 3.236241e6

QD
type: SiteQuality
SIO_000300: 2.398e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.36e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.09e0

FS
type: SiteQuality
SIO_000300: 5.28e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.31e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
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variant carriers: 0

GenotypeQuality
all individuals: 259
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variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563232765358762e-5
allele num: 63970
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.265822784810127e-3
allele num: 790
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 4.02e-1

DP
type: SiteQuality
SIO_000300: 2.621698e6

FS
type: SiteQuality
SIO_000300: 4.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.73e-1

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1699
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variant carriers: 0

GenotypeQuality
all individuals: 2994
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.341372044017794e-4
allele num: 8542
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63972
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9370
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

FS
type: SiteQuality
SIO_000300: 7.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.498e1

DP
type: SiteQuality
SIO_000300: 2.621499e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.93e0

GenotypeQuality
all individuals: 53
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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
all individuals: 2855
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GenotypeQuality
all individuals: 3065
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63946
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.074575542660649e-4
allele num: 9306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.81e0

VQSLOD
type: SiteQuality
SIO_000300: -1.171e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: -1.087e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.14e0

DP
type: SiteQuality
SIO_000300: 2.618322e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-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
all individuals: 207
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563770563582911e-5
allele num: 63948
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 9.73e0

QD
type: SiteQuality
SIO_000300: 1.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.53e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

DP
type: SiteQuality
SIO_000300: 2.617005e6

VQSLOD
type: SiteQuality
SIO_000300: -1.364e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 2890
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564064064064064e-5
allele num: 63936
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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allele num: 788
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.615937e6

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.269e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.12e-1

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

African
type: Population
allele count: 1
allele frequency: 1.021450459652707e-4
allele num: 9790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63936
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9252
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 788
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQ
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.699e0

QD
type: SiteQuality
SIO_000300: 1.411e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1674
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GenotypeQuality
all individuals: 2950
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.70928409684724e-4
allele num: 11482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9174
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

QD
type: SiteQuality
SIO_000300: 1.694e1

DP
type: SiteQuality
SIO_000300: 2.611676e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.861e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 3.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.62e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32743
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 85
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564945226917058e-5
allele num: 63900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

QD
type: SiteQuality
SIO_000300: 7.42e0

DP
type: SiteQuality
SIO_000300: 2.610869e6

FS
type: SiteQuality
SIO_000300: 3.326e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.043e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.18e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: -4.6e-3

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 233
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GenotypeQuality
all individuals: 2803
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564945226917058e-5
allele num: 63900
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.151e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 1.2824e1

DP
type: SiteQuality
SIO_000300: 2.61008e6

MQRankSum
type: SiteQuality
SIO_000300: 1.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.658e0

QD
type: SiteQuality
SIO_000300: 1.331e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -7.46e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 15

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9148
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17343346632246e-4
allele num: 8522
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.025430680885972e-4
allele num: 9752
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.045478306325144e-3
allele num: 11478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.565484204264379e-5
allele num: 63878
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e0

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.608776e6

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

QD
type: SiteQuality
SIO_000300: 1.108e1

GenotypeQuality
all individuals: 800
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 536
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GenotypeQuality
all individuals: 4497
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.336898395721925e-3
allele num: 9724
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9112
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 3.273e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.265e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.59e-1

DP
type: SiteQuality
SIO_000300: 2.605709e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

GenotypeQuality
all individuals: 1552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3575
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3391
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GenotypeQuality
all individuals: 1462
bin: 2.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535437906891045e-5
allele num: 65128
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.632e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.846e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.374435e6

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.23e-1

QD
type: SiteQuality
SIO_000300: 1.489e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.308e0

DP
type: SiteQuality
SIO_000300: 1.379807e6

VQSLOD
type: SiteQuality
SIO_000300: 5.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.556e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.558117793705204e-4
allele num: 6418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531956614988664e-5
allele num: 65276
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15344
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.483e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.03e-1

MQ
type: SiteQuality
SIO_000300: 5.914e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

DP
type: SiteQuality
SIO_000300: 1.388561e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15318
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
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Latino
type: Population
allele count: 1
allele frequency: 8.841732979664014e-5
allele num: 11310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65272
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
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.05e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.978e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

DP
type: SiteQuality
SIO_000300: 1.393971e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9408
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15318
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.841732979664014e-5
allele num: 11310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65272
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

MQ
type: SiteQuality
SIO_000300: 6.05e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

DP
type: SiteQuality
SIO_000300: 1.393971e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

FS
type: SiteQuality
SIO_000300: 1.978e0

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

MQRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.247e1

GenotypeQuality
all individuals: 348
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1491
bin: 7.75e1
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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 5.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38705
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15518
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.796622097114708e-5
allele num: 11368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.638719139574676e-5
allele num: 65456
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

DP
type: SiteQuality
SIO_000300: 1.448604e6

MQRankSum
type: SiteQuality
SIO_000300: -2.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.036e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

QD
type: SiteQuality
SIO_000300: 1.292e1

GenotypeQuality
all individuals: 145
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
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GenotypeQuality
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GenotypeQuality
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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: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1859
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.576240161083654e-5
allele num: 65556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15642
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.341e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.19e0

FS
type: SiteQuality
SIO_000300: 4.486e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 1.464172e6

MQ
type: SiteQuality
SIO_000300: 5.923e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
all individuals: 280
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 190
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15772
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9496
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522579859313621e-5
allele num: 65678
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -9.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.635e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

FS
type: SiteQuality
SIO_000300: 9.587999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.054e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.483505e6

GenotypeQuality
all individuals: 328
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
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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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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.174364040503828e-5
allele num: 16196
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66022
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.329e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

VQSLOD
type: SiteQuality
SIO_000300: 8.93e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.429e0

DP
type: SiteQuality
SIO_000300: 1.521197e6

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 308
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 97
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GenotypeQuality
all individuals: 116
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.69414014953921e-5
allele num: 11502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51372952680815e-5
allele num: 66062
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.24e0

FS
type: SiteQuality
SIO_000300: 1.399e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

DP
type: SiteQuality
SIO_000300: 1.524406e6

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

QD
type: SiteQuality
SIO_000300: 1.171e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509206157561123e-5
allele num: 66260
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.928e0

DP
type: SiteQuality
SIO_000300: 1.538532e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.03e-1

FS
type: SiteQuality
SIO_000300: 2.817e0

QD
type: SiteQuality
SIO_000300: 1.556e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.542697e6

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 2.363e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66420
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16498
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.546627e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 1.099e1

FS
type: SiteQuality
SIO_000300: 7.442e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-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
all individuals: 1986
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 97
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GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010416039496658e-5
allele num: 66436
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.548105e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.09e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.15e-1

FS
type: SiteQuality
SIO_000300: 7.479e0

VQSLOD
type: SiteQuality
SIO_000300: 5.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.49e-1

GenotypeQuality
all individuals: 375
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45003
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 914
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1990
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505162708088744e-5
allele num: 66438
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 3.508e0

DP
type: SiteQuality
SIO_000300: 1.548439e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

QD
type: SiteQuality
SIO_000300: 1.22e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1980
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44766
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8164
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 993
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 909
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66456
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.276102088167053e-3
allele num: 8620
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

DP
type: SiteQuality
SIO_000300: 1.548891e6

VQSLOD
type: SiteQuality
SIO_000300: 8.110000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.63e-1

MQ
type: SiteQuality
SIO_000300: 5.894e1

FS
type: SiteQuality
SIO_000300: 3.184e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

QD
type: SiteQuality
SIO_000300: 1.075e1

GenotypeQuality
all individuals: 985
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 374
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1978
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1819
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44518
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 128
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505570611261668e-5
allele num: 66420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.16e0

QD
type: SiteQuality
SIO_000300: 1.042e1

FS
type: SiteQuality
SIO_000300: 8.093e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.812e-1

DP
type: SiteQuality
SIO_000300: 1.547607e6

GenotypeQuality
all individuals: 336
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8032
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1750
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44252
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 8.25e1
variant carriers: 1

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

South Asian
type: Population
allele count: 16
allele frequency: 9.693444807948625e-4
allele num: 16506
num of homozygotes: 0

East Asian
type: Population
allele count: 697
allele frequency: 8.089600742804086e-2
allele num: 8616
num of homozygotes: 26

European (Non-Finnish)
type: Population
allele count: 39
allele frequency: 5.871725383920506e-4
allele num: 66420
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 5.605381165919282e-3
allele num: 892
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.056343820686819e-4
allele num: 9726
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.31e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

DP
type: SiteQuality
SIO_000300: 1.584439e6

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 119
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8195
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 855
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44952
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.25e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.515610791148833e-4
allele num: 6598
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.03e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
type: SiteQuality
SIO_000300: 1.550331e6

QD
type: SiteQuality
SIO_000300: 1.219e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

FS
type: SiteQuality
SIO_000300: 2.695e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

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

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8152
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1762
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.597402597402597e-4
allele num: 11550
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.247191011235955e-3
allele num: 890
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 130
allele frequency: 1.97089144936325e-2
allele num: 6596
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 6.023370678231539e-4
allele num: 66408
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.4e0

QD
type: SiteQuality
SIO_000300: 1.167e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

DP
type: SiteQuality
SIO_000300: 1.556089e6

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

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 151
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8175
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 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: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505933377507379e-5
allele num: 66404
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.057189878625797e-4
allele num: 9722
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.99e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
SIO_000300: 1.209e1

DP
type: SiteQuality
SIO_000300: 1.550247e6

FS
type: SiteQuality
SIO_000300: 2.467e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.78e-1

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 8.75e1
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GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1771
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44899
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1948
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8165
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50652324565368e-5
allele num: 66378
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.83e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

DP
type: SiteQuality
SIO_000300: 1.548598e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.283e0

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-3

QD
type: SiteQuality
SIO_000300: 1.772e1

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 164
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8150
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44686
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9700
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.059e-1

DP
type: SiteQuality
SIO_000300: 1.547319e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.837e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.4e-2

FS
type: SiteQuality
SIO_000300: 5.787e0

QD
type: SiteQuality
SIO_000300: 6.87e0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1936
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 905
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8140
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.73460537727667e-4
allele num: 11530
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.34e-1

QD
type: SiteQuality
SIO_000300: 8.220000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

FS
type: SiteQuality
SIO_000300: 4.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.12e-1

DP
type: SiteQuality
SIO_000300: 1.546402e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.8e-1

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1765
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508022680661117e-5
allele num: 66312
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.195e1

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

DP
type: SiteQuality
SIO_000300: 1.545449e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 777
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1930
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8142
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44659
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 903
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508113651444773e-5
allele num: 66308
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

FS
type: SiteQuality
SIO_000300: 1.244e0

QD
type: SiteQuality
SIO_000300: 1.337e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.559e0

DP
type: SiteQuality
SIO_000300: 1.544631e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e-1

GenotypeQuality
all individuals: 1757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
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variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44401
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8096
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66278
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.52e-1

QD
type: SiteQuality
SIO_000300: 1.002e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: -5.82e-1

DP
type: SiteQuality
SIO_000300: 1.54143e6

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7986
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66138
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.147113594040968e-4
allele num: 8592
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 1.53429e6

FS
type: SiteQuality
SIO_000300: 5.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.04e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43023
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.027550711474417e-5
allele num: 66060
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.322e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

DP
type: SiteQuality
SIO_000300: 1.52995e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.88e0

GenotypeQuality
all individuals: 1734
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 414
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7920
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 122
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 904
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 167
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.428953121204761e-4
allele num: 16468
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.028742768876639e-5
allele num: 66034
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.527152e6

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.006e0

QD
type: SiteQuality
SIO_000300: 1.017e1

GenotypeQuality
all individuals: 1736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7880
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 9.75e1
variant carriers: 60

GenotypeQuality
all individuals: 250
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42520
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

African
type: Population
allele count: 52
allele frequency: 5.424577508867098e-3
allele num: 9586
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.854773957060569e-4
allele num: 11458
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515059693351918e-5
allele num: 66004
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.525592e6

MQRankSum
type: SiteQuality
SIO_000300: 3.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.43e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

GenotypeQuality
all individuals: 440
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 250
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1881
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7920
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42743
bin: 6.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514646632940535e-5
allele num: 66022
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.76e-1

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

DP
type: SiteQuality
SIO_000300: 1.524455e6

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.4e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

FS
type: SiteQuality
SIO_000300: 7.146e0

GenotypeQuality
all individuals: 229
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3236
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 804
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7459
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.25e1
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GenotypeQuality
all individuals: 336
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39989
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1675
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523275651961979e-5
allele num: 65648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.111e0

MQ
type: SiteQuality
SIO_000300: 5.859e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.64e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.359e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.27e-1

DP
type: SiteQuality
SIO_000300: 1.495167e6

QD
type: SiteQuality
SIO_000300: 9.99e0

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

GenotypeQuality
all individuals: 2063
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4940
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 277
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.538319539734794e-5
allele num: 65006
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11288
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.626e0

FS
type: SiteQuality
SIO_000300: 4.997e0

QD
type: SiteQuality
SIO_000300: 1.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.097e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.446428e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.34e-1

MQ
type: SiteQuality
SIO_000300: 5.82e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.27e-1

GenotypeQuality
all individuals: 515
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3175
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3067
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variant carriers: 0

GenotypeQuality
all individuals: 2792
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variant carriers: 0

GenotypeQuality
all individuals: 309
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variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4623
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variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 258
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variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63146
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.230012300123001e-4
allele num: 16260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.96e-1

FS
type: SiteQuality
SIO_000300: 3.047e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.08e-1

DP
type: SiteQuality
SIO_000300: 1.410189e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.89e0

GenotypeQuality
all individuals: 29026
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
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variant carriers: 0

GenotypeQuality
all individuals: 672
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variant carriers: 0

GenotypeQuality
all individuals: 3167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4422
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1226
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 474
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variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1851
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.153846153846154e-5
allele num: 16250
num of homozygotes: 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: 6144
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9130
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11126
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.405013e6

VQSLOD
type: SiteQuality
SIO_000300: 8.35e-1

FS
type: SiteQuality
SIO_000300: 4.333e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

QD
type: SiteQuality
SIO_000300: 8.59e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 2233
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4865
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1851
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
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variant carriers: 0

GenotypeQuality
all individuals: 3029
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
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variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 1226
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.159358018450651e-5
allele num: 63304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11126
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6144
num of homozygotes: 0

East Asian
type: Population
allele count: 15
allele frequency: 1.778515532368983e-3
allele num: 8434
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 1.405013e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

FS
type: SiteQuality
SIO_000300: 4.333e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

QD
type: SiteQuality
SIO_000300: 8.59e0

GenotypeQuality
all individuals: 435
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4412
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3153
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1864
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 810
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variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6136
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9118
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11108
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: 1
allele frequency: 1.589067217543302e-5
allele num: 62930
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.646e0

QD
type: SiteQuality
SIO_000300: 8.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.643e0

VQSLOD
type: SiteQuality
SIO_000300: -1.98e0

MQRankSum
type: SiteQuality
SIO_000300: 6.01e-1

DP
type: SiteQuality
SIO_000300: 1.401346e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.339e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 1136
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3005
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 811
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 632
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variant carriers: 0

GenotypeQuality
all individuals: 296
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variant carriers: 0

GenotypeQuality
all individuals: 3147
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 1.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.61854201735077e-5
allele num: 61784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8908
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.318e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

DP
type: SiteQuality
SIO_000300: 1.397459e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.227e0

FS
type: SiteQuality
SIO_000300: 2.0626e1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.277e0

QD
type: SiteQuality
SIO_000300: 6.899999999999999e-1

GenotypeQuality
all individuals: 661
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 42201
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 9.25e1
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GenotypeQuality
all individuals: 489
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 803
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variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1581
bin: 7.75e1
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GenotypeQuality
all individuals: 896
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 6627
bin: 6.75e1
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GenotypeQuality
all individuals: 164
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1698
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6298
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South Asian
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allele frequency: 0.0e0
allele num: 16256
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.668476427103463e-5
allele num: 65202
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 1.0146e1

VQSLOD
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SIO_000300: -1.251e0

DP
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SIO_000300: 1.494351e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.14e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-2

GenotypeQuality
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variant carriers: 2

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.070781513895286e-5
allele num: 65130
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6298
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2786e1

MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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MQ
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SIO_000300: 5.959e1

InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.535956747457992e-5
allele num: 65106
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9288
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16196
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 2.101e1

BaseQRankSum
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SIO_000300: -1.382e0

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

VQSLOD
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SIO_000300: -1.733e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

DP
type: SiteQuality
SIO_000300: 1.484662e6

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 1.079680414597279e-4
allele num: 9262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16170
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: 8450
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64994
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.855e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.48e-1

FS
type: SiteQuality
SIO_000300: 7.14e0

DP
type: SiteQuality
SIO_000300: 1.479908e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

QD
type: SiteQuality
SIO_000300: 7.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.678e1

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548467017652524e-5
allele num: 64580
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.117432530999271e-5
allele num: 10968
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9188
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

QD
type: SiteQuality
SIO_000300: 1.024e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.227e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.830000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.455969e6

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8968
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63634
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.310740880979428e-5
allele num: 15846
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10608
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6038
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62706
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5908
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South Asian
type: Population
allele count: 2
allele frequency: 1.276813074565884e-4
allele num: 15664
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8820
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Latino
type: Population
allele count: 1
allele frequency: 9.738994935722633e-5
allele num: 10268
num of homozygotes: 0

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.68e-1

VQSLOD
type: SiteQuality
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DP
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MQ
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.626809825931349e-5
allele num: 61470
num of homozygotes: 0

East Asian
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European (Finnish)
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Latino
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South Asian
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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MQ
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DP
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BaseQRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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Latino
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allele frequency: 1.05797714769361e-4
allele num: 9452
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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Other
type: Population
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QD
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5056
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4716
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1923
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3617
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7072
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.822213125938055e-5
allele num: 14658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57028
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.905e1

DP
type: SiteQuality
SIO_000300: 1.182934e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: 4.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

FS
type: SiteQuality
SIO_000300: 9.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.97e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1