17-1387043-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387043
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387043
    reference: chr 17
allele count: 1
allele frequency: 1.753955168905883e-5
allele num: 57014
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-24T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-24T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-24T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-24T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-24T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-24T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-24T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-24T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-24T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-24T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-24T>C
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9939
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

17-1387044-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387044
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387044
    reference: chr 17
allele count: 1
allele frequency: 1.786543752456498e-5
allele num: 55974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-25T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-25T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-25T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-25T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-25T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-25T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-25T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-25T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-25T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-25T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-25T>C
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

17-1387051-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387051
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387051
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 47934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-32A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-32A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-32A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-32A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-32A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-32A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-32A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-32A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-32A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-32A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-32A>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13041
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22411
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

17-1387054-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387054
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387054
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 45018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-35G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-35G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-35G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-35G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-35G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-35G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-35G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-35G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-35G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-35G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-35G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 22947
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13804
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4596
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

17-1387055-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387055
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387055
    reference: chr 17
allele count: 2
allele frequency: 4.546694553059925e-5
allele num: 43988
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-36C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-36C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-36C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-36C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-36C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-36C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-36C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-36C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-36C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-36C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-36C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11636
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4868
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

17-1387062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387062
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387062
    reference: chr 17
allele count: 6
allele frequency: 1.537830633586221e-4
allele num: 39016
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-43C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-43C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-43C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-43C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-43C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-43C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-43C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-43C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-43C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-43C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-43C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25065
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14770
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9128
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15549
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

17-1387063-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387063
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387063
    reference: chr 17
allele count: 8
allele frequency: 2.079758747985234e-4
allele num: 38466
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-44A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-44A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-44A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-44A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-44A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-44A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-44A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-44A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-44A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-44A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-44A>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25253
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14813
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8892
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14979
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-1387065-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387065
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387065
    reference: chr 17
allele count: 4
allele frequency: 1.076947929567605e-4
allele num: 37142
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-46G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-46G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-46G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-46G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-46G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-46G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-46G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-46G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-46G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-46G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-46G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14853
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25704
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8373
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 9.75e1
  variant carriers: 4
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum

17-1387066-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387066
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387066
    reference: chr 17
allele count: 0
allele frequency: 0.0e0
allele num: 35900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-47C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-47C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-47C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-47C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-47C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-47C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-47C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-47C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-47C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-47C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-47C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26054
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14912
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11652
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

17-1387067-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387067
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387067
    reference: chr 17
allele count: 9
allele frequency: 2.497918401332223e-4
allele num: 36030
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-48T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-48T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-48T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-48T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-48T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-48T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-48T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-48T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-48T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-48T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-48T>C
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26054
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD

17-1387068-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387068
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387068
    reference: chr 17
allele count: 2
allele frequency: 5.55926173004225e-5
allele num: 35976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-49A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-49A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-49A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-49A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-49A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-49A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-49A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-49A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-49A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-49A>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-49A>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14996
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26125
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 9.75e1
  variant carriers: 4
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

17-1387069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387069
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387069
    reference: chr 17
allele count: 3
allele frequency: 8.424599831508003e-5
allele num: 35610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.127-50C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.160-50C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.175-50C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.166-50C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.127-50C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.127-50C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.127-50C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.232-50C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.127-50C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.127-50C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.127-50C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15010
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7775
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26173
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-1387392-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387392
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387392
    reference: chr 17
allele count: 1
allele frequency: 8.357290900581667e-6
allele num: 119656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+50G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+50G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+50G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+50G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+50G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+50G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+50G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+50G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+50G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+50G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+50G>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

17-1387392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387392
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387392
    reference: chr 17
allele count: 1
allele frequency: 8.357290900581667e-6
allele num: 119656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+50G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+50G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+50G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+50G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+50G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+50G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+50G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+50G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+50G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+50G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+50G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4165
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24314
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

17-1387394-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387394
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387394
    reference: chr 17
allele count: 19
allele frequency: 1.588203825063528e-4
allele num: 119632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+48A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+48A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+48A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+48A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+48A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+48A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+48A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+48A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+48A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+48A>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+48A>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4154
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9826
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11297
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8130
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

17-1387394-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387394
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387394
    reference: chr 17
allele count: 676
allele frequency: 5.650662030226026e-3
allele num: 119632
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+48A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+48A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+48A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+48A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+48A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+48A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+48A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+48A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+48A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+48A>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+48A>C
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 4.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 9826
  bin: 2.25e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 1.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 4154
  bin: 3.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 11297
  bin: 3.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 4.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 20522
  bin: 2.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 5.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 9.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 5.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 11066
  bin: 9.75e1
  variant carriers: 645
num of homozygotes: 19
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

17-1387395-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387395
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387395
    reference: chr 17
allele count: 2
allele frequency: 1.671597880413888e-5
allele num: 119646
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+47C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+47C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+47C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+47C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+47C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+47C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+47C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+47C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+47C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+47C>G
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+47C>G
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11262
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

17-1387403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387403
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387403
    reference: chr 17
allele count: 292
allele frequency: 2.439961896485452e-3
allele num: 119674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+39C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+39C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+39C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+39C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+39C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+39C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+39C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+39C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+39C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+39C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+39C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11267
  bin: 3.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 3.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 4.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 20821
  bin: 2.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10781
  bin: 2.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 4
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-1387404-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387404
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387405
    reference: chr 17
allele count: 1
allele frequency: 8.358408559010364e-6
allele num: 119640
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+37dupG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+37dupG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+37dupG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+37dupG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+37dupG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+37dupG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+37dupG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+37dupG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+37dupG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+37dupG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+37dupG
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/17-1387405-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387405
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387405
    reference: chr 17
allele count: 1
allele frequency: 8.356173541012099e-6
allele num: 119672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+37G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+37G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+37G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+37G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+37G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+37G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+37G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+37G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+37G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+37G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+37G>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20994
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10492
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/17-1387412-A-ACC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387412
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387414
    reference: chr 17
allele count: 2
allele frequency: 1.671625823275718e-5
allele num: 119644
alternate allele: ACC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+28_126+29dupGG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+28_126+29dupGG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+28_126+29dupGG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+28_165+29dupGG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+28_159+29dupGG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+28_126+29dupGG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+28_126+29dupGG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+28_174+29dupGG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+28_126+29dupGG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+28_231+29dupGG
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+28_126+29dupGG
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10910
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-1387427-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387427
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387427
    reference: chr 17
allele count: 4
allele frequency: 3.339121143315079e-5
allele num: 119792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+15G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+15G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+15G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+15G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+15G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+15G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+15G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+15G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+15G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+15G>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+15G>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10835
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD

17-1387427-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387427
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387427
    reference: chr 17
allele count: 1
allele frequency: 8.347802858287698e-6
allele num: 119792
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+15G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+15G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

17-1387428-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387428
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387428
    reference: chr 17
allele count: 3
allele frequency: 2.504048211274894e-5
allele num: 119806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+14G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+14G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+14G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+14G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+14G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+14G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+14G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+14G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+14G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+14G>A
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+14G>A
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11379
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

17-1387429-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387429
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387429
    reference: chr 17
allele count: 3
allele frequency: 2.50388101557414e-5
allele num: 119814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+13T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+13T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+13T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+13T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+13T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+13T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+13T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+13T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+13T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+13T>C
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+13T>C
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10908
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28149
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

17-1387435-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387435
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387435
    reference: chr 17
allele count: 2
allele frequency: 1.668529858341815e-5
allele num: 119866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126+7C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231+7C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126+7C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126+7C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126+7C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159+7C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174+7C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126+7C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165+7C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126+7C>T
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126+7C>T
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.231+7C>T
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

17-1387442-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387442
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387442
    reference: chr 17
allele count: 1
allele frequency: 8.339448929214757e-6
allele num: 119912
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.174C>T
  hgvsp: ENST00000438665.2:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.126C>T
  hgvsp: ENST00000361007.2:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.126C>T
  hgvsp: ENST00000571715.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.126C>T
  hgvsp: ENST00000575158.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.126C>T
  hgvsp: ENST00000574790.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.231C>T
  hgvsp: ENST00000359786.5:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.126C>T
  hgvsp: ENST00000573853.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.126C>T
  hgvsp: ENST00000575335.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.165C>T
  hgvsp: ENST00000570490.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.126C>T
  hgvsp: ENST00000570984.2:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.159C>T
  hgvsp: ENST00000545534.2:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.231C>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

17-1387449-A-ACCACTCCCAGTTGGGGAATAAGTCATGGGTGT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387449
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387481
    reference: chr 17
allele count: 1
allele frequency: 8.337502084375522e-6
allele num: 119940
alternate allele: ACCACTCCCAGTTGGGGAATAAGTCATGGGTGT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsp: ENSP00000461175.1:p.Leu40HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsp: ENSP00000460831.1:p.Leu40HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsp: ENSP00000458610.1:p.Leu40HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsp: ENSP00000459271.2:p.Leu40HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsp: ENSP00000412197.2:p.Leu56HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsp: ENSP00000460415.1:p.Leu40HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsp: ENSP00000437685.2:p.Leu51HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsp: ENSP00000459174.1:p.Leu40HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsp: ENSP00000354283.2:p.Leu40HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsp: ENSP00000352834.5:p.Leu75HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsp: ENSP00000461682.1:p.Leu53HisfsTer73
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3056
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu75HisfsTer73
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

17-1387450-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387450
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387450
    reference: chr 17
allele count: 4
allele frequency: 3.334889615153738e-5
allele num: 119944
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.157C>A
  hgvsp: ENSP00000461682.1:p.Leu53Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.118C>A
  hgvsp: ENSP00000354283.2:p.Leu40Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.166C>A
  hgvsp: ENSP00000412197.2:p.Leu56Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.118C>A
  hgvsp: ENSP00000460415.1:p.Leu40Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.118C>A
  hgvsp: ENSP00000461175.1:p.Leu40Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.118C>A
  hgvsp: ENSP00000458610.1:p.Leu40Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.223C>A
  hgvsp: ENSP00000352834.5:p.Leu75Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.118C>A
  hgvsp: ENSP00000459174.1:p.Leu40Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.151C>A
  hgvsp: ENSP00000437685.2:p.Leu51Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.118C>A
  hgvsp: ENSP00000459271.2:p.Leu40Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.118C>A
  hgvsp: ENSP00000460831.1:p.Leu40Ile
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11428
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu75Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

17-1387451-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387451
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387451
    reference: chr 17
allele count: 2
allele frequency: 1.667361400583577e-5
allele num: 119950
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.165T>C
  hgvsp: ENST00000438665.2:c.165T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.222T>C
  hgvsp: ENST00000359786.5:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.156T>C
  hgvsp: ENST00000570490.1:c.156T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.117T>C
  hgvsp: ENST00000571715.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.150T>C
  hgvsp: ENST00000545534.2:c.150T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.117T>C
  hgvsp: ENST00000575335.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.117T>C
  hgvsp: ENST00000361007.2:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.117T>C
  hgvsp: ENST00000574790.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.117T>C
  hgvsp: ENST00000573853.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.117T>C
  hgvsp: ENST00000570984.2:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.117T>C
  hgvsp: ENST00000575158.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn74Asn
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

17-1387452-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387452
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387452
    reference: chr 17
allele count: 1
allele frequency: 8.337224037884346e-6
allele num: 119944
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.116A>C
  hgvsp: ENSP00000460831.1:p.Asn39Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.155A>C
  hgvsp: ENSP00000461682.1:p.Asn52Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.116A>C
  hgvsp: ENSP00000460415.1:p.Asn39Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.116A>C
  hgvsp: ENSP00000461175.1:p.Asn39Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.116A>C
  hgvsp: ENSP00000458610.1:p.Asn39Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.149A>C
  hgvsp: ENSP00000437685.2:p.Asn50Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.221A>C
  hgvsp: ENSP00000352834.5:p.Asn74Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.164A>C
  hgvsp: ENSP00000412197.2:p.Asn55Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.116A>C
  hgvsp: ENSP00000354283.2:p.Asn39Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.116A>C
  hgvsp: ENSP00000459174.1:p.Asn39Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.116A>C
  hgvsp: ENSP00000459271.2:p.Asn39Thr
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn74Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

17-1387458-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387458
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387458
    reference: chr 17
allele count: 32
allele frequency: 2.67031609866818e-4
allele num: 119836
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.215G>A
  hgvsp: ENSP00000352834.5:p.Arg72Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.143G>A
  hgvsp: ENSP00000437685.2:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.110G>A
  hgvsp: ENSP00000354283.2:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.158G>A
  hgvsp: ENSP00000412197.2:p.Arg53Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.110G>A
  hgvsp: ENSP00000459174.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.110G>A
  hgvsp: ENSP00000458610.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.110G>A
  hgvsp: ENSP00000461175.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.149G>A
  hgvsp: ENSP00000461682.1:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.110G>A
  hgvsp: ENSP00000460415.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.110G>A
  hgvsp: ENSP00000460831.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.110G>A
  hgvsp: ENSP00000459271.2:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 22050
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11411
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg72Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/17-1387460-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387460
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387460
    reference: chr 17
allele count: 1
allele frequency: 8.341953351796856e-6
allele num: 119876
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.213T>G
  hgvsp: ENSP00000352834.5:p.Phe71Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.108T>G
  hgvsp: ENSP00000458610.1:p.Phe36Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.141T>G
  hgvsp: ENSP00000437685.2:p.Phe47Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.108T>G
  hgvsp: ENSP00000461175.1:p.Phe36Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.147T>G
  hgvsp: ENSP00000461682.1:p.Phe49Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.108T>G
  hgvsp: ENSP00000460415.1:p.Phe36Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.108T>G
  hgvsp: ENSP00000354283.2:p.Phe36Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.108T>G
  hgvsp: ENSP00000459271.2:p.Phe36Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.108T>G
  hgvsp: ENSP00000460831.1:p.Phe36Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.156T>G
  hgvsp: ENSP00000412197.2:p.Phe52Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.108T>G
  hgvsp: ENSP00000459174.1:p.Phe36Leu
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22095
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe71Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

17-1387464-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387464
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387464
    reference: chr 17
allele count: 2
allele frequency: 1.668669069550127e-5
allele num: 119856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.143G>A
  hgvsp: ENSP00000461682.1:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.104G>A
  hgvsp: ENSP00000354283.2:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.104G>A
  hgvsp: ENSP00000460415.1:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.104G>A
  hgvsp: ENSP00000460831.1:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.209G>A
  hgvsp: ENSP00000352834.5:p.Arg70Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.104G>A
  hgvsp: ENSP00000458610.1:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.104G>A
  hgvsp: ENSP00000459174.1:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.152G>A
  hgvsp: ENSP00000412197.2:p.Arg51Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.137G>A
  hgvsp: ENSP00000437685.2:p.Arg46Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.104G>A
  hgvsp: ENSP00000459271.2:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.104G>A
  hgvsp: ENSP00000461175.1:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg70Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

17-1387465-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387465
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387465
    reference: chr 17
allele count: 2
allele frequency: 1.668446342765617e-5
allele num: 119872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.136C>T
  hgvsp: ENSP00000437685.2:p.Arg46Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.142C>T
  hgvsp: ENSP00000461682.1:p.Arg48Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.103C>T
  hgvsp: ENSP00000460415.1:p.Arg35Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.103C>T
  hgvsp: ENSP00000461175.1:p.Arg35Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.151C>T
  hgvsp: ENSP00000412197.2:p.Arg51Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.103C>T
  hgvsp: ENSP00000354283.2:p.Arg35Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.103C>T
  hgvsp: ENSP00000458610.1:p.Arg35Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.103C>T
  hgvsp: ENSP00000459271.2:p.Arg35Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.208C>T
  hgvsp: ENSP00000352834.5:p.Arg70Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.103C>T
  hgvsp: ENSP00000460831.1:p.Arg35Ter
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.103C>T
  hgvsp: ENSP00000459174.1:p.Arg35Ter
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg70Ter
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-1387466-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387466
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387466
    reference: chr 17
allele count: 1
allele frequency: 8.34125752798492e-6
allele num: 119886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.150G>A
  hgvsp: ENST00000438665.2:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.135G>A
  hgvsp: ENST00000545534.2:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.207G>A
  hgvsp: ENST00000359786.5:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.141G>A
  hgvsp: ENST00000570490.1:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.102G>A
  hgvsp: ENST00000575158.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.102G>A
  hgvsp: ENST00000571715.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.102G>A
  hgvsp: ENST00000573853.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.102G>A
  hgvsp: ENST00000570984.2:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.102G>A
  hgvsp: ENST00000574790.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.102G>A
  hgvsp: ENST00000361007.2:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.102G>A
  hgvsp: ENST00000575335.1:c.102G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11391
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg69Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

17-1387467-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387467
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387467
    reference: chr 17
allele count: 1
allele frequency: 8.342231713828083e-6
allele num: 119872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.101G>A
  hgvsp: ENSP00000461175.1:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.149G>A
  hgvsp: ENSP00000412197.2:p.Arg50Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.101G>A
  hgvsp: ENSP00000459174.1:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.101G>A
  hgvsp: ENSP00000458610.1:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.134G>A
  hgvsp: ENSP00000437685.2:p.Arg45Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.206G>A
  hgvsp: ENSP00000352834.5:p.Arg69Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.101G>A
  hgvsp: ENSP00000460831.1:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.140G>A
  hgvsp: ENSP00000461682.1:p.Arg47Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.101G>A
  hgvsp: ENSP00000460415.1:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.101G>A
  hgvsp: ENSP00000354283.2:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.101G>A
  hgvsp: ENSP00000459271.2:p.Arg34Gln
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg69Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

17-1387468-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387468
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387468
    reference: chr 17
allele count: 3
allele frequency: 2.503170682864962e-5
allele num: 119848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.133C>T
  hgvsp: ENSP00000437685.2:p.Arg45Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.100C>T
  hgvsp: ENSP00000459174.1:p.Arg34Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.205C>T
  hgvsp: ENSP00000352834.5:p.Arg69Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.100C>T
  hgvsp: ENSP00000354283.2:p.Arg34Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.100C>T
  hgvsp: ENSP00000460415.1:p.Arg34Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.139C>T
  hgvsp: ENSP00000461682.1:p.Arg47Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.148C>T
  hgvsp: ENSP00000412197.2:p.Arg50Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.100C>T
  hgvsp: ENSP00000459271.2:p.Arg34Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.100C>T
  hgvsp: ENSP00000461175.1:p.Arg34Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.100C>T
  hgvsp: ENSP00000458610.1:p.Arg34Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.100C>T
  hgvsp: ENSP00000460831.1:p.Arg34Trp
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10802
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg69Trp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/17-1387470-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387470
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387470
    reference: chr 17
allele count: 1
allele frequency: 8.342231713828083e-6
allele num: 119872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.131G>T
  hgvsp: ENSP00000437685.2:p.Arg44Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.98G>T
  hgvsp: ENSP00000461175.1:p.Arg33Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.98G>T
  hgvsp: ENSP00000460415.1:p.Arg33Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.146G>T
  hgvsp: ENSP00000412197.2:p.Arg49Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.98G>T
  hgvsp: ENSP00000458610.1:p.Arg33Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.203G>T
  hgvsp: ENSP00000352834.5:p.Arg68Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.137G>T
  hgvsp: ENSP00000461682.1:p.Arg46Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.98G>T
  hgvsp: ENSP00000354283.2:p.Arg33Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.98G>T
  hgvsp: ENSP00000459174.1:p.Arg33Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.98G>T
  hgvsp: ENSP00000460831.1:p.Arg33Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.98G>T
  hgvsp: ENSP00000459271.2:p.Arg33Leu
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11430
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg68Leu
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: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

17-1387470-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387470
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387470
    reference: chr 17
allele count: 9
allele frequency: 7.508008542445276e-5
allele num: 119872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.98G>A
  hgvsp: ENSP00000354283.2:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.98G>A
  hgvsp: ENSP00000461175.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.98G>A
  hgvsp: ENSP00000460415.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.137G>A
  hgvsp: ENSP00000461682.1:p.Arg46Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.98G>A
  hgvsp: ENSP00000460831.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.203G>A
  hgvsp: ENSP00000352834.5:p.Arg68Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.131G>A
  hgvsp: ENSP00000437685.2:p.Arg44Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.98G>A
  hgvsp: ENSP00000459174.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.98G>A
  hgvsp: ENSP00000459271.2:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.98G>A
  hgvsp: ENSP00000458610.1:p.Arg33Gln
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.146G>A
  hgvsp: ENSP00000412197.2:p.Arg49Gln
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22134
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg68Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

17-1387471-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387471
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387471
    reference: chr 17
allele count: 4
allele frequency: 3.336391692384686e-5
allele num: 119890
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.97C>T
  hgvsp: ENSP00000458610.1:p.Arg33Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.97C>T
  hgvsp: ENSP00000459174.1:p.Arg33Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.97C>T
  hgvsp: ENSP00000354283.2:p.Arg33Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.136C>T
  hgvsp: ENSP00000461682.1:p.Arg46Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.97C>T
  hgvsp: ENSP00000461175.1:p.Arg33Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.97C>T
  hgvsp: ENSP00000460831.1:p.Arg33Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.130C>T
  hgvsp: ENSP00000437685.2:p.Arg44Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.97C>T
  hgvsp: ENSP00000459271.2:p.Arg33Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.202C>T
  hgvsp: ENSP00000352834.5:p.Arg68Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.145C>T
  hgvsp: ENSP00000412197.2:p.Arg49Trp
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.97C>T
  hgvsp: ENSP00000460415.1:p.Arg33Trp
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11433
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22180
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg68Trp
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: FS

17-1387472-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387472
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387472
    reference: chr 17
allele count: 13401
allele frequency: 1.116973394678936e-1
allele num: 119976
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.96G>A
  hgvsp: ENST00000575335.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.96G>A
  hgvsp: ENST00000574790.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.96G>A
  hgvsp: ENST00000570984.2:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.129G>A
  hgvsp: ENST00000545534.2:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.96G>A
  hgvsp: ENST00000575158.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.201G>A
  hgvsp: ENST00000359786.5:c.201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.96G>A
  hgvsp: ENST00000573853.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.96G>A
  hgvsp: ENST00000361007.2:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.144G>A
  hgvsp: ENST00000438665.2:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.96G>A
  hgvsp: ENST00000571715.1:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.135G>A
  hgvsp: ENST00000570490.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10595
  bin: 3.25e1
  variant carriers: 1218
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.25e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 21073
  bin: 2.75e1
  variant carriers: 940
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.75e1
  variant carriers: 280
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 6.25e1
  variant carriers: 789
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 3.75e1
  variant carriers: 1317
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.75e1
  variant carriers: 265
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 6.75e1
  variant carriers: 554
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 4.25e1
  variant carriers: 1320
genotype depth: GenotypeDepth
  all individuals: 9779
  bin: 2.25e1
  variant carriers: 522
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 7.5e0
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.75e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 9.75e1
  variant carriers: 1074
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 4.75e1
  variant carriers: 1289
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 5.25e1
  variant carriers: 1135
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.25e1
  variant carriers: 392
genotype quality: GenotypeQuality
hgvs: p.Leu67Leu
num of homozygotes: 889
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

17-1387481-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387481
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387481
    reference: chr 17
allele count: 2
allele frequency: 1.669281874937402e-5
allele num: 119812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.126C>T
  hgvsp: ENST00000570490.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.87C>T
  hgvsp: ENST00000574790.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.87C>T
  hgvsp: ENST00000571715.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.192C>T
  hgvsp: ENST00000359786.5:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.135C>T
  hgvsp: ENST00000438665.2:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.120C>T
  hgvsp: ENST00000545534.2:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.87C>T
  hgvsp: ENST00000570984.2:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.87C>T
  hgvsp: ENST00000575335.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.87C>T
  hgvsp: ENST00000361007.2:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.87C>T
  hgvsp: ENST00000573853.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.87C>T
  hgvsp: ENST00000575158.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile64Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

17-1387484-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387484
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387484
    reference: chr 17
allele count: 601
allele frequency: 5.015187422811175e-3
allele num: 119836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.123C>T
  hgvsp: ENST00000570490.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.132C>T
  hgvsp: ENST00000438665.2:c.132C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.117C>T
  hgvsp: ENST00000545534.2:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.189C>T
  hgvsp: ENST00000359786.5:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.84C>T
  hgvsp: ENST00000574790.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.84C>T
  hgvsp: ENST00000571715.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.84C>T
  hgvsp: ENST00000570984.2:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.84C>T
  hgvsp: ENST00000575335.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.84C>T
  hgvsp: ENST00000361007.2:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.84C>T
  hgvsp: ENST00000573853.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.84C>T
  hgvsp: ENST00000575158.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25313
  bin: 2.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 11086
  bin: 2.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 6.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 5.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12001
  bin: 3.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 4.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 4.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
hgvs: p.Phe63Phe
num of homozygotes: 9
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

17-1387487-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387487
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387487
    reference: chr 17
allele count: 1
allele frequency: 8.348499774590506e-6
allele num: 119782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.114C>G
  hgvsp: ENST00000545534.2:c.114C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.81C>G
  hgvsp: ENST00000574790.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.120C>G
  hgvsp: ENST00000570490.1:c.120C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.81C>G
  hgvsp: ENST00000571715.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.81C>G
  hgvsp: ENST00000575335.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.81C>G
  hgvsp: ENST00000575158.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.186C>G
  hgvsp: ENST00000359786.5:c.186C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.129C>G
  hgvsp: ENST00000438665.2:c.129C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.81C>G
  hgvsp: ENST00000361007.2:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.81C>G
  hgvsp: ENST00000570984.2:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.81C>G
  hgvsp: ENST00000573853.1:c.81C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12091
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala62Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ

17-1387488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387488
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387488
    reference: chr 17
allele count: 7
allele frequency: 5.844828162052035e-5
allele num: 119764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.80C>T
  hgvsp: ENSP00000458610.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.119C>T
  hgvsp: ENSP00000461682.1:p.Ala40Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.80C>T
  hgvsp: ENSP00000461175.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.80C>T
  hgvsp: ENSP00000459271.2:p.Ala27Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.185C>T
  hgvsp: ENSP00000352834.5:p.Ala62Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.80C>T
  hgvsp: ENSP00000460415.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.80C>T
  hgvsp: ENSP00000459174.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.128C>T
  hgvsp: ENSP00000412197.2:p.Ala43Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.80C>T
  hgvsp: ENSP00000354283.2:p.Ala27Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.113C>T
  hgvsp: ENSP00000437685.2:p.Ala38Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.80C>T
  hgvsp: ENSP00000460831.1:p.Ala27Val
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala62Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

17-1387489-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387489
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387489
    reference: chr 17
allele count: 1
allele frequency: 8.351149118118652e-6
allele num: 119744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.79G>A
  hgvsp: ENSP00000459174.1:p.Ala27Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.127G>A
  hgvsp: ENSP00000412197.2:p.Ala43Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.79G>A
  hgvsp: ENSP00000354283.2:p.Ala27Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.79G>A
  hgvsp: ENSP00000460831.1:p.Ala27Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.184G>A
  hgvsp: ENSP00000352834.5:p.Ala62Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.112G>A
  hgvsp: ENSP00000437685.2:p.Ala38Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.79G>A
  hgvsp: ENSP00000459271.2:p.Ala27Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.79G>A
  hgvsp: ENSP00000458610.1:p.Ala27Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.118G>A
  hgvsp: ENSP00000461682.1:p.Ala40Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.79G>A
  hgvsp: ENSP00000460415.1:p.Ala27Thr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.79G>A
  hgvsp: ENSP00000461175.1:p.Ala27Thr
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala62Thr
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

17-1387491-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387491
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387491
    reference: chr 17
allele count: 1
allele frequency: 8.350730688935283e-6
allele num: 119750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.116C>T
  hgvsp: ENSP00000461682.1:p.Ala39Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.77C>T
  hgvsp: ENSP00000354283.2:p.Ala26Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.125C>T
  hgvsp: ENSP00000412197.2:p.Ala42Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.77C>T
  hgvsp: ENSP00000461175.1:p.Ala26Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.182C>T
  hgvsp: ENSP00000352834.5:p.Ala61Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.110C>T
  hgvsp: ENSP00000437685.2:p.Ala37Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.77C>T
  hgvsp: ENSP00000459174.1:p.Ala26Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.77C>T
  hgvsp: ENSP00000458610.1:p.Ala26Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.77C>T
  hgvsp: ENSP00000460415.1:p.Ala26Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.77C>T
  hgvsp: ENSP00000459271.2:p.Ala26Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.77C>T
  hgvsp: ENSP00000460831.1:p.Ala26Val
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12026
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala61Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

17-1387493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387493
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387493
    reference: chr 17
allele count: 1
allele frequency: 8.350451759440186e-6
allele num: 119754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.75G>A
  hgvsp: ENST00000570984.2:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.108G>A
  hgvsp: ENST00000545534.2:c.108G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.75G>A
  hgvsp: ENST00000361007.2:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.123G>A
  hgvsp: ENST00000438665.2:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.75G>A
  hgvsp: ENST00000574790.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.180G>A
  hgvsp: ENST00000359786.5:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.75G>A
  hgvsp: ENST00000571715.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.75G>A
  hgvsp: ENST00000575335.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.75G>A
  hgvsp: ENST00000575158.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.114G>A
  hgvsp: ENST00000570490.1:c.114G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.75G>A
  hgvsp: ENST00000573853.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu60Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

17-1387496-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387496
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387496
    reference: chr 17
allele count: 61
allele frequency: 5.094881731925699e-4
allele num: 119728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.72C>T
  hgvsp: ENST00000573853.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.111C>T
  hgvsp: ENST00000570490.1:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.72C>T
  hgvsp: ENST00000570984.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.105C>T
  hgvsp: ENST00000545534.2:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.177C>T
  hgvsp: ENST00000359786.5:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.72C>T
  hgvsp: ENST00000361007.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.120C>T
  hgvsp: ENST00000438665.2:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.72C>T
  hgvsp: ENST00000571715.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.72C>T
  hgvsp: ENST00000574790.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.72C>T
  hgvsp: ENST00000575335.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.72C>T
  hgvsp: ENST00000575158.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 25431
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ser59Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

17-1387503-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387503
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387503
    reference: chr 17
allele count: 1
allele frequency: 8.355196096452384e-6
allele num: 119686
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.65T>C
  hgvsp: ENSP00000460831.1:p.Phe22Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.65T>C
  hgvsp: ENSP00000458610.1:p.Phe22Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.104T>C
  hgvsp: ENSP00000461682.1:p.Phe35Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.65T>C
  hgvsp: ENSP00000459271.2:p.Phe22Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.65T>C
  hgvsp: ENSP00000461175.1:p.Phe22Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.65T>C
  hgvsp: ENSP00000459174.1:p.Phe22Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.113T>C
  hgvsp: ENSP00000412197.2:p.Phe38Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.65T>C
  hgvsp: ENSP00000354283.2:p.Phe22Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.170T>C
  hgvsp: ENSP00000352834.5:p.Phe57Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.98T>C
  hgvsp: ENSP00000437685.2:p.Phe33Ser
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.65T>C
  hgvsp: ENSP00000460415.1:p.Phe22Ser
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe57Ser
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

17-1387509-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387509
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387509
    reference: chr 17
allele count: 1
allele frequency: 8.357849692431131e-6
allele num: 119648
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.164A>G
  hgvsp: ENSP00000352834.5:p.Glu55Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.59A>G
  hgvsp: ENSP00000460831.1:p.Glu20Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.59A>G
  hgvsp: ENSP00000354283.2:p.Glu20Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.107A>G
  hgvsp: ENSP00000412197.2:p.Glu36Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.59A>G
  hgvsp: ENSP00000461175.1:p.Glu20Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.59A>G
  hgvsp: ENSP00000460415.1:p.Glu20Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.59A>G
  hgvsp: ENSP00000459174.1:p.Glu20Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.92A>G
  hgvsp: ENSP00000437685.2:p.Glu31Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.59A>G
  hgvsp: ENSP00000458610.1:p.Glu20Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.98A>G
  hgvsp: ENSP00000461682.1:p.Glu33Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.59A>G
  hgvsp: ENSP00000459271.2:p.Glu20Gly
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu55Gly
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

17-1387513-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387513
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387513
    reference: chr 17
allele count: 1
allele frequency: 8.362462577979963e-6
allele num: 119582
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.55C>G
  hgvsp: ENSP00000354283.2:p.Leu19Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.94C>G
  hgvsp: ENSP00000461682.1:p.Leu32Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.55C>G
  hgvsp: ENSP00000459271.2:p.Leu19Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.55C>G
  hgvsp: ENSP00000458610.1:p.Leu19Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.88C>G
  hgvsp: ENSP00000437685.2:p.Leu30Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.55C>G
  hgvsp: ENSP00000461175.1:p.Leu19Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.55C>G
  hgvsp: ENSP00000459174.1:p.Leu19Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.160C>G
  hgvsp: ENSP00000352834.5:p.Leu54Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.55C>G
  hgvsp: ENSP00000460415.1:p.Leu19Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.55C>G
  hgvsp: ENSP00000460831.1:p.Leu19Val
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.103C>G
  hgvsp: ENSP00000412197.2:p.Leu35Val
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu54Val
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/17-1387518-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387518
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387518
    reference: chr 17
allele count: 1
allele frequency: 8.365680631776201e-6
allele num: 119536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.50T>G
  hgvsp: ENSP00000461175.1:p.Val17Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.50T>G
  hgvsp: ENSP00000460415.1:p.Val17Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.98T>G
  hgvsp: ENSP00000412197.2:p.Val33Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.89T>G
  hgvsp: ENSP00000461682.1:p.Val30Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.50T>G
  hgvsp: ENSP00000458610.1:p.Val17Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.50T>G
  hgvsp: ENSP00000354283.2:p.Val17Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.83T>G
  hgvsp: ENSP00000437685.2:p.Val28Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.50T>G
  hgvsp: ENSP00000459174.1:p.Val17Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.155T>G
  hgvsp: ENSP00000352834.5:p.Val52Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.50T>G
  hgvsp: ENSP00000459271.2:p.Val17Gly
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.50T>G
  hgvsp: ENSP00000460831.1:p.Val17Gly
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25385
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11817
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val52Gly
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/17-1387519-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387519
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387519
    reference: chr 17
allele count: 3
allele frequency: 2.510376221716428e-5
allele num: 119504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.49G>T
  hgvsp: ENSP00000460831.1:p.Val17Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.97G>T
  hgvsp: ENSP00000412197.2:p.Val33Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.49G>T
  hgvsp: ENSP00000459174.1:p.Val17Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.49G>T
  hgvsp: ENSP00000459271.2:p.Val17Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.154G>T
  hgvsp: ENSP00000352834.5:p.Val52Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.49G>T
  hgvsp: ENSP00000460415.1:p.Val17Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.49G>T
  hgvsp: ENSP00000461175.1:p.Val17Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.88G>T
  hgvsp: ENSP00000461682.1:p.Val30Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.82G>T
  hgvsp: ENSP00000437685.2:p.Val28Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.49G>T
  hgvsp: ENSP00000458610.1:p.Val17Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.49G>T
  hgvsp: ENSP00000354283.2:p.Val17Leu
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val52Leu
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum

17-1387519-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387519
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387519
    reference: chr 17
allele count: 2
allele frequency: 1.673584147810952e-5
allele num: 119504
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.154G>A
  hgvsp: ENSP00000352834.5:p.Val52Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.49G>A
  hgvsp: ENSP00000458610.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.82G>A
  hgvsp: ENSP00000437685.2:p.Val28Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.97G>A
  hgvsp: ENSP00000412197.2:p.Val33Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.49G>A
  hgvsp: ENSP00000459174.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.49G>A
  hgvsp: ENSP00000459271.2:p.Val17Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.49G>A
  hgvsp: ENSP00000460415.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.49G>A
  hgvsp: ENSP00000461175.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.49G>A
  hgvsp: ENSP00000354283.2:p.Val17Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.49G>A
  hgvsp: ENSP00000460831.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.88G>A
  hgvsp: ENSP00000461682.1:p.Val30Met
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11847
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val52Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

17-1387520-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387520
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387520
    reference: chr 17
allele count: 7
allele frequency: 5.857740585774059e-5
allele num: 119500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.48C>T
  hgvsp: ENST00000361007.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.48C>T
  hgvsp: ENST00000570984.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.81C>T
  hgvsp: ENST00000545534.2:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.48C>T
  hgvsp: ENST00000574790.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.153C>T
  hgvsp: ENST00000359786.5:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.48C>T
  hgvsp: ENST00000573853.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.48C>T
  hgvsp: ENST00000575158.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.87C>T
  hgvsp: ENST00000570490.1:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.96C>T
  hgvsp: ENST00000438665.2:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.48C>T
  hgvsp: ENST00000575335.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.48C>T
  hgvsp: ENST00000571715.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Phe51Phe
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

17-1387526-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387526
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387526
    reference: chr 17
allele count: 2
allele frequency: 1.675041876046901e-5
allele num: 119400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.42G>A
  hgvsp: ENST00000575335.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.75G>A
  hgvsp: ENST00000545534.2:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.81G>A
  hgvsp: ENST00000570490.1:c.81G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.147G>A
  hgvsp: ENST00000359786.5:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.90G>A
  hgvsp: ENST00000438665.2:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.42G>A
  hgvsp: ENST00000574790.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.42G>A
  hgvsp: ENST00000570984.2:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.42G>A
  hgvsp: ENST00000575158.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.42G>A
  hgvsp: ENST00000571715.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.42G>A
  hgvsp: ENST00000361007.2:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.42G>A
  hgvsp: ENST00000573853.1:c.42G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln49Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/17-1387531-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387531
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387531
    reference: chr 17
allele count: 1
allele frequency: 8.384759860477596e-6
allele num: 119264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.37G>T
  hgvsp: ENSP00000458610.1:p.Val13Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.37G>T
  hgvsp: ENSP00000461175.1:p.Val13Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.76G>T
  hgvsp: ENSP00000461682.1:p.Val26Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.142G>T
  hgvsp: ENSP00000352834.5:p.Val48Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.37G>T
  hgvsp: ENSP00000460415.1:p.Val13Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.37G>T
  hgvsp: ENSP00000354283.2:p.Val13Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.85G>T
  hgvsp: ENSP00000412197.2:p.Val29Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.37G>T
  hgvsp: ENSP00000459271.2:p.Val13Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.70G>T
  hgvsp: ENSP00000437685.2:p.Val24Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.37G>T
  hgvsp: ENSP00000459174.1:p.Val13Leu
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.37G>T
  hgvsp: ENSP00000460831.1:p.Val13Leu
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val48Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

17-1387534-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387534
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387534
    reference: chr 17
allele count: 1
allele frequency: 8.388839487945237e-6
allele num: 119206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.73G>A
  hgvsp: ENSP00000461682.1:p.Gly25Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.34G>A
  hgvsp: ENSP00000460415.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.67G>A
  hgvsp: ENSP00000437685.2:p.Gly23Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.82G>A
  hgvsp: ENSP00000412197.2:p.Gly28Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.34G>A
  hgvsp: ENSP00000458610.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.34G>A
  hgvsp: ENSP00000459271.2:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.139G>A
  hgvsp: ENSP00000352834.5:p.Gly47Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.34G>A
  hgvsp: ENSP00000461175.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.34G>A
  hgvsp: ENSP00000460831.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.34G>A
  hgvsp: ENSP00000459174.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.34G>A
  hgvsp: ENSP00000354283.2:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11764
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly47Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/17-1387535-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387535
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387535
    reference: chr 17
allele count: 1
allele frequency: 8.389824820457749e-6
allele num: 119192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.66G>T
  hgvsp: ENST00000545534.2:c.66G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.138G>T
  hgvsp: ENST00000359786.5:c.138G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.33G>T
  hgvsp: ENST00000575335.1:c.33G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.33G>T
  hgvsp: ENST00000573853.1:c.33G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.33G>T
  hgvsp: ENST00000571715.1:c.33G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.33G>T
  hgvsp: ENST00000361007.2:c.33G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.33G>T
  hgvsp: ENST00000574790.1:c.33G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.72G>T
  hgvsp: ENST00000570490.1:c.72G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.33G>T
  hgvsp: ENST00000575158.1:c.33G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.81G>T
  hgvsp: ENST00000438665.2:c.81G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.33G>T
  hgvsp: ENST00000570984.2:c.33G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val46Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

17-1387538-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387538
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387538
    reference: chr 17
allele count: 255
allele frequency: 2.140195387249471e-3
allele num: 119148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.30G>A
  hgvsp: ENST00000571715.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.30G>A
  hgvsp: ENST00000570984.2:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.30G>A
  hgvsp: ENST00000575158.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.135G>A
  hgvsp: ENST00000359786.5:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.78G>A
  hgvsp: ENST00000438665.2:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.63G>A
  hgvsp: ENST00000545534.2:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.30G>A
  hgvsp: ENST00000574790.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.30G>A
  hgvsp: ENST00000575335.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.69G>A
  hgvsp: ENST00000570490.1:c.69G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.30G>A
  hgvsp: ENST00000573853.1:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.30G>A
  hgvsp: ENST00000361007.2:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11697
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 11141
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 25451
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
hgvs: p.Arg45Arg
num of homozygotes: 4
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-1387543-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387543
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387543
    reference: chr 17
allele count: 1
allele frequency: 8.39630562552477e-6
allele num: 119100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.25G>T
  hgvsp: ENSP00000461175.1:p.Asp9Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.73G>T
  hgvsp: ENSP00000412197.2:p.Asp25Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.130G>T
  hgvsp: ENSP00000352834.5:p.Asp44Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.64G>T
  hgvsp: ENSP00000461682.1:p.Asp22Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.25G>T
  hgvsp: ENSP00000459174.1:p.Asp9Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.58G>T
  hgvsp: ENSP00000437685.2:p.Asp20Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.25G>T
  hgvsp: ENSP00000460415.1:p.Asp9Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.25G>T
  hgvsp: ENSP00000354283.2:p.Asp9Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.25G>T
  hgvsp: ENSP00000458610.1:p.Asp9Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.25G>T
  hgvsp: ENSP00000459271.2:p.Asp9Tyr
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.25G>T
  hgvsp: ENSP00000460831.1:p.Asp9Tyr
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp44Tyr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

17-1387545-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387545
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387545
    reference: chr 17
allele count: 1
allele frequency: 8.40039649871474e-6
allele num: 119042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.56G>A
  hgvsp: ENSP00000437685.2:p.Arg19His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.23G>A
  hgvsp: ENSP00000460415.1:p.Arg8His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.23G>A
  hgvsp: ENSP00000459271.2:p.Arg8His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.23G>A
  hgvsp: ENSP00000459174.1:p.Arg8His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.62G>A
  hgvsp: ENSP00000461682.1:p.Arg21His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.23G>A
  hgvsp: ENSP00000354283.2:p.Arg8His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.128G>A
  hgvsp: ENSP00000352834.5:p.Arg43His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.23G>A
  hgvsp: ENSP00000461175.1:p.Arg8His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.71G>A
  hgvsp: ENSP00000412197.2:p.Arg24His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.23G>A
  hgvsp: ENSP00000460831.1:p.Arg8His
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.23G>A
  hgvsp: ENSP00000458610.1:p.Arg8His
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg43His
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
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: VQSLOD
site quality: ClippingRankSum

17-1387546-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387546
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387546
    reference: chr 17
allele count: 9
allele frequency: 7.562643900307548e-5
allele num: 119006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.22C>T
  hgvsp: ENSP00000459271.2:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.22C>T
  hgvsp: ENSP00000460415.1:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.127C>T
  hgvsp: ENSP00000352834.5:p.Arg43Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.22C>T
  hgvsp: ENSP00000461175.1:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.61C>T
  hgvsp: ENSP00000461682.1:p.Arg21Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.22C>T
  hgvsp: ENSP00000460831.1:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.70C>T
  hgvsp: ENSP00000412197.2:p.Arg24Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.22C>T
  hgvsp: ENSP00000459174.1:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.55C>T
  hgvsp: ENSP00000437685.2:p.Arg19Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.22C>T
  hgvsp: ENSP00000354283.2:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.22C>T
  hgvsp: ENSP00000458610.1:p.Arg8Cys
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11670
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25471
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg43Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP

17-1387550-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387550
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387550
    reference: chr 17
allele count: 7
allele frequency: 5.886607127840288e-5
allele num: 118914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.18C>T
  hgvsp: ENST00000573853.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.18C>T
  hgvsp: ENST00000574790.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.51C>T
  hgvsp: ENST00000545534.2:c.51C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.57C>T
  hgvsp: ENST00000570490.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.18C>T
  hgvsp: ENST00000570984.2:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.18C>T
  hgvsp: ENST00000575158.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.66C>T
  hgvsp: ENST00000438665.2:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.18C>T
  hgvsp: ENST00000361007.2:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.18C>T
  hgvsp: ENST00000575335.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.123C>T
  hgvsp: ENST00000359786.5:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.18C>T
  hgvsp: ENST00000571715.1:c.18C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11627
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr41Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-1387553-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387553
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387553
    reference: chr 17
allele count: 5
allele frequency: 4.206275763439051e-5
allele num: 118870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.54C>T
  hgvsp: ENST00000570490.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.48C>T
  hgvsp: ENST00000545534.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.120C>T
  hgvsp: ENST00000359786.5:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.15C>T
  hgvsp: ENST00000361007.2:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.15C>T
  hgvsp: ENST00000570984.2:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.15C>T
  hgvsp: ENST00000574790.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.15C>T
  hgvsp: ENST00000571715.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.63C>T
  hgvsp: ENST00000438665.2:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.15C>T
  hgvsp: ENST00000575158.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.15C>T
  hgvsp: ENST00000573853.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.15C>T
  hgvsp: ENST00000575335.1:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu40Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD

17-1387555-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1387555
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 1387555
    reference: chr 17
allele count: 3
allele frequency: 2.523807921391796e-5
allele num: 118868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000354283
  ensembl transcript: ENST00000361007
  gene symbol: MYO1C
  hgvsc: ENST00000361007.2:c.13C>A
  hgvsp: ENSP00000354283.2:p.Leu5Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461682
  ensembl transcript: ENST00000570490
  gene symbol: MYO1C
  hgvsc: ENST00000570490.1:c.52C>A
  hgvsp: ENSP00000461682.1:p.Leu18Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000458610
  ensembl transcript: ENST00000571715
  gene symbol: MYO1C
  hgvsc: ENST00000571715.1:c.13C>A
  hgvsp: ENSP00000458610.1:p.Leu5Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000352834
  ensembl transcript: ENST00000359786
  gene symbol: MYO1C
  hgvsc: ENST00000359786.5:c.118C>A
  hgvsp: ENSP00000352834.5:p.Leu40Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000437685
  ensembl transcript: ENST00000545534
  gene symbol: MYO1C
  hgvsc: ENST00000545534.2:c.46C>A
  hgvsp: ENSP00000437685.2:p.Leu16Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000461175
  ensembl transcript: ENST00000574790
  gene symbol: MYO1C
  hgvsc: ENST00000574790.1:c.13C>A
  hgvsp: ENSP00000461175.1:p.Leu5Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459271
  ensembl transcript: ENST00000570984
  gene symbol: MYO1C
  hgvsc: ENST00000570984.2:c.13C>A
  hgvsp: ENSP00000459271.2:p.Leu5Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000412197
  ensembl transcript: ENST00000438665
  gene symbol: MYO1C
  hgvsc: ENST00000438665.2:c.61C>A
  hgvsp: ENSP00000412197.2:p.Leu21Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460415
  ensembl transcript: ENST00000575335
  gene symbol: MYO1C
  hgvsc: ENST00000575335.1:c.13C>A
  hgvsp: ENSP00000460415.1:p.Leu5Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000459174
  ensembl transcript: ENST00000575158
  gene symbol: MYO1C
  hgvsc: ENST00000575158.1:c.13C>A
  hgvsp: ENSP00000459174.1:p.Leu5Ile
  variant of: http://identifiers.org/hgnc/7597
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000197879
  ensembl protein: ENSP00000460831
  ensembl transcript: ENST00000573853
  gene symbol: MYO1C
  hgvsc: ENST00000573853.1:c.13C>A
  hgvsp: ENSP00000460831.1:p.Leu5Ile
  variant of: http://identifiers.org/hgnc/7597
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11499
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11567
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu40Ile
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 2104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1865
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2576
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10666
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5920
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2280
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28952
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.298805832288711e-5
allele num: 30314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3330
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.15e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.88e0

DP
type: SiteQuality
SIO_000300: 7.11739e5

ClippingRankSum
type: SiteQuality
SIO_000300: 8.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.545e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.667e1

GenotypeQuality
all individuals: 1419
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2587
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28077
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2159
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11208
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5688
bin: 6.25e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3190
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.36337952374546e-5
allele num: 29732
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3250
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.24e-2

FS
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SIO_000300: 0.0e0

VQSLOD
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DP
type: SiteQuality
SIO_000300: 7.039e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.59e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.292e1

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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GenotypeQuality
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2252
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

DP
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FS
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MQRankSum
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BaseQRankSum
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SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
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QD
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SIO_000300: 1.42e1

MQ
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 7.36e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 23030
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2786
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2000
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

QD
type: SiteQuality
SIO_000300: 1.776e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

MQRankSum
type: SiteQuality
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DP
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SIO_000300: 6.42794e5

VQSLOD
type: SiteQuality
SIO_000300: -1.016e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9514
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.279831045406547e-4
allele num: 1894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.469473496022169e-5
allele num: 22374
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4308
num of homozygotes: 0

East Asian
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: 362
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2710
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.16e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

BaseQRankSum
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SIO_000300: -1.031e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-1

DP
type: SiteQuality
SIO_000300: 6.35407e5

QD
type: SiteQuality
SIO_000300: 9.59e0

VQSLOD
type: SiteQuality
SIO_000300: 2.79e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2388
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 1.032737787875658e-4
allele num: 19366
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9164
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1372
num of homozygotes: 0

European (Finnish)
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allele count: 4
allele frequency: 1.6e-3
allele num: 2500
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.01577e5

FS
type: SiteQuality
SIO_000300: 5.807e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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QD
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SIO_000300: 1.701e1

ReadPosRankSum
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MQRankSum
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SIO_000300: -4.77e-1

ClippingRankSum
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SIO_000300: 7.31e-1

BaseQRankSum
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SIO_000300: -1.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.32e-2

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 2342
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9114
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African
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allele count: 8
allele frequency: 2.070393374741201e-3
allele num: 3864
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 19020
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
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European (Finnish)
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 7.84e0

VQSLOD
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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Other
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num of homozygotes: 0

South Asian
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African
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 4
allele frequency: 2.193704069321049e-4
allele num: 18234
num of homozygotes: 0

VQSLOD
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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MQ
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 1132
num of homozygotes: 0

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

East Asian
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African
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Other
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South Asian
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European (Finnish)
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FS
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BaseQRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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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: 15

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 495
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variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8910
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 2.191780821917808e-3
allele num: 3650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2160
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.728689275893676e-5
allele num: 17456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2396
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

QD
type: SiteQuality
SIO_000300: 1.625e1

MQ
type: SiteQuality
SIO_000300: 5.672e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.62e-2

FS
type: SiteQuality
SIO_000300: 3.929e0

DP
type: SiteQuality
SIO_000300: 5.90469e5

VQSLOD
type: SiteQuality
SIO_000300: 3.12e-1

GenotypeQuality
all individuals: 8640
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8906
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.146263182026593e-4
allele num: 17448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2384
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.89587e5

VQSLOD
type: SiteQuality
SIO_000300: -4.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.612e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.53e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.662e1

GenotypeQuality
all individuals: 7347
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 495
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GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.741149158444574e-4
allele num: 17230
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1136
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.187e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 5.89067e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.58e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.78e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 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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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 94
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 24314
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65524
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169317118802619e-4
allele num: 8552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.916e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.986e0

DP
type: SiteQuality
SIO_000300: 1.920096e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.9e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

QD
type: SiteQuality
SIO_000300: 9.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.19e-1

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 94
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169317118802619e-4
allele num: 8552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.9e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.986e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.916e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.19e-1

QD
type: SiteQuality
SIO_000300: 9.5e0

MQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e-1

DP
type: SiteQuality
SIO_000300: 1.920096e6

GenotypeQuality
all individuals: 976
bin: 2.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 19

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053714844107857e-5
allele num: 65494
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.222222222222222e-3
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 9.120758847136082e-4
allele num: 16446
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

FS
type: SiteQuality
SIO_000300: 8.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.47e-2

QD
type: SiteQuality
SIO_000300: 1.256e1

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.661e0

DP
type: SiteQuality
SIO_000300: 1.922069e6

GenotypeQuality
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bin: 6.25e1
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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bin: 3.25e1
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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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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 19
allele frequency: 2.222222222222222e-3
allele num: 8550
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.478865889719951e-4
allele num: 11498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053714844107857e-5
allele num: 65494
num of homozygotes: 0

South Asian
type: Population
allele count: 650
allele frequency: 3.952328833758969e-2
allele num: 16446
num of homozygotes: 19

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.39e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.47e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-2

DP
type: SiteQuality
SIO_000300: 1.922069e6

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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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
all individuals: 10604
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.053621595211921e-5
allele num: 65496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.358e1

VQSLOD
type: SiteQuality
SIO_000300: 3.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 1.914754e6

FS
type: SiteQuality
SIO_000300: 1.093e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 1007
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1096
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8268
bin: 6.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2949
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 591
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2174
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3166
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26768
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10758
bin: 9.75e1
variant carriers: 284

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.220963951039345e-4
allele num: 65522
num of homozygotes: 0

African
type: Population
allele count: 273
allele frequency: 2.686479039559142e-2
allele num: 10162
num of homozygotes: 4

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.077549532028686e-5
allele num: 16454
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.697164724299878e-4
allele num: 11498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.278e1

MQ
type: SiteQuality
SIO_000300: 5.933e1

DP
type: SiteQuality
SIO_000300: 1.920131e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.073e0

FS
type: SiteQuality
SIO_000300: 1.404e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.38e-2

GenotypeQuality
all individuals: 107
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26546
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variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2947
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3160
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1097
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10491
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
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: 898
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526857422053929e-5
allele num: 65494
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.916637e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

FS
type: SiteQuality
SIO_000300: 6.621e0

MQ
type: SiteQuality
SIO_000300: 6.016e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

QD
type: SiteQuality
SIO_000300: 1.304e1

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

GenotypeQuality
all individuals: 3162
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1416
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8288
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2948
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26913
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2168
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526251526251526e-5
allele num: 65520
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.529999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.99e-1

DP
type: SiteQuality
SIO_000300: 1.918055e6

GenotypeQuality
all individuals: 3095
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27378
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2914
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10488
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1412
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1096
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8271
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526717557251908e-5
allele num: 65500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.369999999999999e0

DP
type: SiteQuality
SIO_000300: 1.922503e6

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

FS
type: SiteQuality
SIO_000300: 4.49e0

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.799e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.55e-1

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

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27952
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10489
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2925
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3084
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.429543245869776e-4
allele num: 16464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.745e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.931015e6

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

QD
type: SiteQuality
SIO_000300: 1.157e1

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10489
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27952
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3084
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
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variant carriers: 0

GenotypeQuality
all individuals: 8272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
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variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

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

GenotypeQuality
all individuals: 2925
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2140
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1089
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.02e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.06e-1

DP
type: SiteQuality
SIO_000300: 1.931015e6

FS
type: SiteQuality
SIO_000300: 5.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.745e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

QD
type: SiteQuality
SIO_000300: 1.157e1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

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

GenotypeQuality
all individuals: 1054
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3079
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 1090
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variant carriers: 0

GenotypeQuality
all individuals: 1410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8273
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variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10491
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 370
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2136
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.607335303320007e-4
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.142e0

MQ
type: SiteQuality
SIO_000300: 5.91e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: -6.814e-1

FS
type: SiteQuality
SIO_000300: 4.561e0

QD
type: SiteQuality
SIO_000300: 9.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.931075e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.02e-1

GenotypeQuality
all individuals: 1057
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2927
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variant carriers: 0

GenotypeQuality
all individuals: 164
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variant carriers: 0

GenotypeQuality
all individuals: 73
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variant carriers: 0

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

GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 1409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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Latino
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MQ
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FS
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Other
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South Asian
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DP
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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QD
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MQ
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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Other
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East Asian
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VQSLOD
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FS
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ReadPosRankSum
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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MQ
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SIO_000300: 5.888e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

East Asian
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Latino
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African
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European (Non-Finnish)
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Other
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South Asian
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MQ
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VQSLOD
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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MQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Other
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Latino
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European (Non-Finnish)
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European (Finnish)
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African
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MQ
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QD
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FS
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DP
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.047665488236011e-5
allele num: 65624
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

South Asian
type: Population
allele count: 30
allele frequency: 1.821714840903571e-3
allele num: 16468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.05e1

FS
type: SiteQuality
SIO_000300: 5.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.461e-1

DP
type: SiteQuality
SIO_000300: 1.936096e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.887e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.18e-1

GenotypeDepth
all individuals: 475
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8096
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variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.25e1
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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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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 379
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variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65646
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.934577e6

MQ
type: SiteQuality
SIO_000300: 5.551e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

QD
type: SiteQuality
SIO_000300: 9.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: -9.898e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.94e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 468
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

GenotypeQuality
all individuals: 1410
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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: 11506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.047294002925402e-5
allele num: 65632
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.351e0

MQ
type: SiteQuality
SIO_000300: 5.825e1

QD
type: SiteQuality
SIO_000300: 1.566e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.68e-1

FS
type: SiteQuality
SIO_000300: 1.0729e1

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

DP
type: SiteQuality
SIO_000300: 1.934704e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.177e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
all individuals: 816
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variant carriers: 0

GenotypeQuality
all individuals: 1061
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 938
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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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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: 2

GenotypeQuality
all individuals: 28015
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GenotypeQuality
all individuals: 427
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523322060750084e-5
allele num: 65646
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.167406023815083e-4
allele num: 8566
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 2.447e0

DP
type: SiteQuality
SIO_000300: 1.934876e6

MQRankSum
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SIO_000300: -3.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.777e-1

QD
type: SiteQuality
SIO_000300: 1.733e1

MQ
type: SiteQuality
SIO_000300: 5.915e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeDepth
all individuals: 280
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variant carriers: 0

GenotypeQuality
all individuals: 2109
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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: 1409
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8081
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variant carriers: 0

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 375
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10479
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GenotypeQuality
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GenotypeQuality
all individuals: 357
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variant carriers: 0

GenotypeQuality
all individuals: 130
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variant carriers: 0

GenotypeQuality
all individuals: 2849
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523136442562525e-5
allele num: 65654
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

QD
type: SiteQuality
SIO_000300: 1.382e1

VQSLOD
type: SiteQuality
SIO_000300: -1.27e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.907e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

FS
type: SiteQuality
SIO_000300: 3.352e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

DP
type: SiteQuality
SIO_000300: 1.935685e6

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
all individuals: 161
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16795141322121e-4
allele num: 8562
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
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SIO_000300: -1.452e0

DP
type: SiteQuality
SIO_000300: 1.936234e6

QD
type: SiteQuality
SIO_000300: 2.968e1

GenotypeDepth
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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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GenotypeQuality
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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: 145
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GenotypeQuality
all individuals: 2108
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.047201145747631e-5
allele num: 65634
num of homozygotes: 0

African
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South Asian
type: Population
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

ClippingRankSum
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MQ
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VQSLOD
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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QD
type: SiteQuality
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MQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1067
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523136442562525e-5
allele num: 65654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.93717e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.912e1

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

QD
type: SiteQuality
SIO_000300: 1.285e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

FS
type: SiteQuality
SIO_000300: 5.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

GenotypeDepth
all individuals: 339
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8029
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variant carriers: 0

GenotypeQuality
all individuals: 2865
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28260
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variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 7.5e0
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GenotypeQuality
all individuals: 346
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2111
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 10485
bin: 9.75e1
variant carriers: 9

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1408
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
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variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.21850915405002e-4
allele num: 65654
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.23e-1

MQ
type: SiteQuality
SIO_000300: 5.912e1

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 1.93717e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

QD
type: SiteQuality
SIO_000300: 1.285e1

GenotypeDepth
all individuals: 1108
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 960
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GenotypeQuality
all individuals: 28516
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 2109
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
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variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.568156900962358e-5
allele num: 65672
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.792401096748923e-5
allele num: 10212
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.223e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 1.937637e6

QD
type: SiteQuality
SIO_000300: 1.254e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 3.217e0

GenotypeDepth
all individuals: 1549
bin: 5.75e1
variant carriers: 943

GenotypeQuality
all individuals: 156
bin: 4.25e1
variant carriers: 14

GenotypeQuality
all individuals: 596
bin: 8.75e1
variant carriers: 38

GenotypeQuality
all individuals: 2289
bin: 7.75e1
variant carriers: 50

GenotypeQuality
all individuals: 1381
bin: 8.25e1
variant carriers: 39

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 26908
bin: 6.25e1
variant carriers: 42

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 21

GenotypeQuality
all individuals: 226
bin: 4.75e1
variant carriers: 26

GenotypeQuality
all individuals: 254
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 21

GenotypeQuality
all individuals: 225
bin: 3.75e1
variant carriers: 8

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 807
bin: 2.25e1
variant carriers: 9

GenotypeQuality
all individuals: 71
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 831
bin: 9.25e1
variant carriers: 54

GenotypeQuality
all individuals: 2218
bin: 7.25e1
variant carriers: 25

GenotypeQuality
all individuals: 7009
bin: 6.75e1
variant carriers: 35

GenotypeQuality
all individuals: 235
bin: 3.25e1
variant carriers: 14

GenotypeQuality
all individuals: 17040
bin: 9.75e1
variant carriers: 12152

African
type: Population
allele count: 752
allele frequency: 7.349491790461297e-2
allele num: 10232
num of homozygotes: 31

South Asian
type: Population
allele count: 1195
allele frequency: 7.252093700691832e-2
allele num: 16478
num of homozygotes: 57

European (Non-Finnish)
type: Population
allele count: 9694
allele frequency: 1.47486611489776e-1
allele num: 65728
num of homozygotes: 708

European (Finnish)
type: Population
allele count: 856
allele frequency: 1.302891933028919e-1
allele num: 6570
num of homozygotes: 63

East Asian
type: Population
allele count: 222
allele frequency: 2.591036414565826e-2
allele num: 8568
num of homozygotes: 4

Latino
type: Population
allele count: 562
allele frequency: 4.884408134886147e-2
allele num: 11506
num of homozygotes: 18

Other
type: Population
allele count: 120
allele frequency: 1.342281879194631e-1
allele num: 894
num of homozygotes: 8

BaseQRankSum
type: SiteQuality
SIO_000300: -3.023e0

DP
type: SiteQuality
SIO_000300: 2.140234e6

MQ
type: SiteQuality
SIO_000300: 5.909e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

QD
type: SiteQuality
SIO_000300: 1.31e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.33e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

GenotypeDepth
all individuals: 874
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6107
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 719
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2848
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8908
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33121
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2969
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
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variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65618
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.739432944859976e-4
allele num: 11498
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.367e1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 1.834944e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.89e0

GenotypeDepth
all individuals: 3242
bin: 3.75e1
variant carriers: 72

GenotypeQuality
all individuals: 202
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 335
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variant carriers: 0

GenotypeQuality
all individuals: 33288
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variant carriers: 0

GenotypeQuality
all individuals: 264
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variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2826
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variant carriers: 1

GenotypeQuality
all individuals: 274
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GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 971
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variant carriers: 0

GenotypeQuality
all individuals: 8861
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
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GenotypeQuality
all individuals: 6389
bin: 9.75e1
variant carriers: 588

GenotypeQuality
all individuals: 308
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1763
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2926
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 1

Latino
type: Population
allele count: 306
allele frequency: 2.661332405635763e-2
allele num: 11498
num of homozygotes: 4

South Asian
type: Population
allele count: 4
allele frequency: 2.426889940541196e-4
allele num: 16482
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.619860404157395e-5
allele num: 65618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

East Asian
type: Population
allele count: 281
allele frequency: 3.275058275058275e-2
allele num: 8580
num of homozygotes: 4

Other
type: Population
allele count: 3
allele frequency: 3.348214285714286e-3
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.96078431372549e-4
allele num: 10200
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.2e0

MQRankSum
type: SiteQuality
SIO_000300: 3.59e-1

QD
type: SiteQuality
SIO_000300: 1.241e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.64e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.172e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.97e-1

DP
type: SiteQuality
SIO_000300: 1.841561e6

GenotypeDepth
all individuals: 832
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33255
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2958
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 1765
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variant carriers: 0

GenotypeQuality
all individuals: 208
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variant carriers: 0

GenotypeQuality
all individuals: 333
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variant carriers: 0

GenotypeQuality
all individuals: 1009
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variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
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variant carriers: 0

GenotypeQuality
all individuals: 446
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GenotypeQuality
all individuals: 695
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GenotypeQuality
all individuals: 91
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variant carriers: 0

GenotypeQuality
all individuals: 5823
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 362
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 979
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variant carriers: 0

GenotypeQuality
all individuals: 2842
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8942
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.809691975671964e-5
allele num: 10194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 2.209e1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.699999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 1.826583e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.324e0

FS
type: SiteQuality
SIO_000300: 1.412e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 107
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variant carriers: 0

GenotypeQuality
all individuals: 320
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variant carriers: 0

GenotypeQuality
all individuals: 1762
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 2840
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GenotypeQuality
all individuals: 90
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GenotypeQuality
all individuals: 363
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GenotypeQuality
all individuals: 1009
bin: 2.25e1
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GenotypeQuality
all individuals: 5823
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variant carriers: 7

GenotypeQuality
all individuals: 224
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GenotypeQuality
all individuals: 342
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variant carriers: 0

GenotypeQuality
all individuals: 33251
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
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variant carriers: 0

GenotypeQuality
all individuals: 8939
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2954
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.067398597133272e-4
allele num: 65580
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.302e1

FS
type: SiteQuality
SIO_000300: 1.756e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.686e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.94e-1

DP
type: SiteQuality
SIO_000300: 1.826494e6

MQ
type: SiteQuality
SIO_000300: 5.884e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

GenotypeDepth
all individuals: 12082
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33165
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2939
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5811
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 250
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1012
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 977
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65578
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: 5.52e-1

FS
type: SiteQuality
SIO_000300: 2.682e0

QD
type: SiteQuality
SIO_000300: 1.168e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.129999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.826605e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e-1

GenotypeDepth
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8889
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variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
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GenotypeQuality
all individuals: 690
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variant carriers: 0

GenotypeQuality
all individuals: 5812
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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 3.25e1
variant carriers: 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: 8566
num of homozygotes: 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: 10194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
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: 1.524808636516117e-5
allele num: 65582
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.75e-1

FS
type: SiteQuality
SIO_000300: 1.317e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.711e0

DP
type: SiteQuality
SIO_000300: 1.825492e6

QD
type: SiteQuality
SIO_000300: 9.1e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 691
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variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
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variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1047
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5810
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 33442
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variant carriers: 0

GenotypeQuality
all individuals: 1745
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65590
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: 8568
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.70170553428472e-5
allele num: 11492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.376e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.242e1

MQRankSum
type: SiteQuality
SIO_000300: 5.76e-1

FS
type: SiteQuality
SIO_000300: 8.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.84e-1

DP
type: SiteQuality
SIO_000300: 1.825086e6

GenotypeDepth
all individuals: 11997
bin: 3.25e1
variant carriers: 8

GenotypeQuality
all individuals: 2786
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 98
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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: 1731
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 214
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 5845
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variant carriers: 61

GenotypeQuality
all individuals: 1078
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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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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
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: 8564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.574146921599122e-5
allele num: 65586
num of homozygotes: 0

African
type: Population
allele count: 50
allele frequency: 4.90869821323385e-3
allele num: 10186
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.963788300835655e-4
allele num: 11488
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

QD
type: SiteQuality
SIO_000300: 1.354e1

DP
type: SiteQuality
SIO_000300: 1.825406e6

GenotypeDepth
all individuals: 1397
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variant carriers: 0

GenotypeQuality
all individuals: 158
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 143
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 38
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 959
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variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.704735376044568e-5
allele num: 11488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65548
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
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MQRankSum
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DP
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.117e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.858e1

VQSLOD
type: SiteQuality
SIO_000300: -8.834e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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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: 179
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525832341542311e-5
allele num: 65538
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: 8566
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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MQRankSum
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DP
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SIO_000300: 1.822141e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 316
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GenotypeQuality
all individuals: 261
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 278
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1709
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GenotypeQuality
all individuals: 2867
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GenotypeQuality
all individuals: 194
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GenotypeQuality
all individuals: 677
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GenotypeQuality
all individuals: 5775
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 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: 1.526484506182262e-5
allele num: 65510
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 1.228e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.821201e6

MQRankSum
type: SiteQuality
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VQSLOD
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

South Asian
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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: 892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.541782300339192e-4
allele num: 6486
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65488
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-2

QD
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InbreedingCoeff
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SIO_000300: 1.9e-3

BaseQRankSum
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SIO_000300: 4.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.933e0

VQSLOD
type: SiteQuality
SIO_000300: -4.43e-2

DP
type: SiteQuality
SIO_000300: 1.819117e6

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

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

South Asian
type: Population
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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.582951420714941e-5
allele num: 65460
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

VQSLOD
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QD
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SIO_000300: 1.222e1

BaseQRankSum
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SIO_000300: 8.129999999999999e-1

MQRankSum
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SIO_000300: 4.65e-1

MQ
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SIO_000300: 5.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

FS
type: SiteQuality
SIO_000300: 5.19e-1

DP
type: SiteQuality
SIO_000300: 1.818755e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.055300947143294e-5
allele num: 65460
num of homozygotes: 0

South Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.96e-1

InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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FS
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SIO_000300: 5.19e-1

BaseQRankSum
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SIO_000300: 8.129999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.222e1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeDepth
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variant carriers: 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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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

South Asian
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allele count: 7
allele frequency: 4.252217227554368e-4
allele num: 16462
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

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

African
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
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num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.924e1

DP
type: SiteQuality
SIO_000300: 1.819118e6

InbreedingCoeff
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SIO_000300: 1.6e-3

MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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SIO_000300: 3.291e0

ClippingRankSum
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SIO_000300: 4.24e-1

QD
type: SiteQuality
SIO_000300: 1.175e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.057542958478566e-5
allele num: 65412
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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BaseQRankSum
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SIO_000300: -1.816e0

FS
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MQRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.530690341343946e-5
allele num: 65330
num of homozygotes: 0

South Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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East Asian
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InbreedingCoeff
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DP
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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QD
type: SiteQuality
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 65310
num of homozygotes: 0

South Asian
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Other
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East Asian
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European (Finnish)
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MQ
type: SiteQuality
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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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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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2776
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8547
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 3.25e1
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GenotypeQuality
all individuals: 949
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33507
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531252871099133e-5
allele num: 65306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.617e0

DP
type: SiteQuality
SIO_000300: 1.813508e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.474e0

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

GenotypeDepth
all individuals: 3121
bin: 3.75e1
variant carriers: 38

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

GenotypeQuality
all individuals: 651
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5927
bin: 9.75e1
variant carriers: 250

GenotypeQuality
all individuals: 235
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8486
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 344
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
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GenotypeQuality
all individuals: 33787
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.5e0
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GenotypeQuality
all individuals: 380
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 398
bin: 3.25e1
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GenotypeQuality
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2732
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2611
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 244
allele frequency: 2.409162717219589e-2
allele num: 10128
num of homozygotes: 4

Latino
type: Population
allele count: 9
allele frequency: 7.843820812271222e-4
allele num: 11474
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.077549532028686e-5
allele num: 16454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531675039823551e-5
allele num: 65288
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.049e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.36e-1

DP
type: SiteQuality
SIO_000300: 1.816771e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-2

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

QD
type: SiteQuality
SIO_000300: 1.419e1

MQRankSum
type: SiteQuality
SIO_000300: 4.38e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 3077
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2738
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34269
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 2598
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variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8425
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5680
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532003554248246e-5
allele num: 65274
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 1.810643e6

MQ
type: SiteQuality
SIO_000300: 5.917e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.853e0

QD
type: SiteQuality
SIO_000300: 6.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.01e-1

FS
type: SiteQuality
SIO_000300: 1.238e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeDepth
all individuals: 1010
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8410
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 248
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5679
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34299
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2589
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10112
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53275497378989e-5
allele num: 65242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

DP
type: SiteQuality
SIO_000300: 1.810129e6

FS
type: SiteQuality
SIO_000300: 1.852e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: -4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: -1.819e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

GenotypeDepth
all individuals: 823
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5680
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 8393
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65212
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.955696202531646e-4
allele num: 10112
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.360718646432932e-4
allele num: 11466
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

FS
type: SiteQuality
SIO_000300: 1.103e0

QD
type: SiteQuality
SIO_000300: 1.346e1

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

DP
type: SiteQuality
SIO_000300: 1.810233e6

GenotypeDepth
all individuals: 158
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
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variant carriers: 0

GenotypeQuality
all individuals: 2557
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variant carriers: 0

GenotypeQuality
all individuals: 2708
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variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8409
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 932
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
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variant carriers: 0

GenotypeQuality
all individuals: 5674
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 299
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1626
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34304
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6314
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.073916111810009e-4
allele num: 65182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.903e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

DP
type: SiteQuality
SIO_000300: 1.807995e6

FS
type: SiteQuality
SIO_000300: 1.1839e1

VQSLOD
type: SiteQuality
SIO_000300: -7.433999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.171e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.53e-1

GenotypeDepth
all individuals: 1005
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5667
bin: 9.75e1
variant carriers: 5

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

GenotypeQuality
all individuals: 379
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variant carriers: 0

GenotypeQuality
all individuals: 1622
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variant carriers: 0

GenotypeQuality
all individuals: 8409
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34509
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2549
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2709
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 5.75e1
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GenotypeQuality
all individuals: 654
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1721
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 932
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 4.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6314
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10066
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.672477289467223e-5
allele num: 65168
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.44e-1

FS
type: SiteQuality
SIO_000300: 3.233e0

VQSLOD
type: SiteQuality
SIO_000300: 6.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.697e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.95e-1

DP
type: SiteQuality
SIO_000300: 1.806738e6

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

QD
type: SiteQuality
SIO_000300: 1.296e1

GenotypeDepth
all individuals: 107
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2549
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2714
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0